ENST00000350026.11:c.3046G>T
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ENSP00000055163.8:p.Ala1016Ser
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ENST00000414678.8:c.2956G>T
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ENSP00000412835.3:p.Ala986Ser
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ENST00000637015.2:c.3046G>T
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ENSP00000489729.2:p.Ala1016Ser
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ENST00000319584.11:c.1060G>T
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ENSP00000313006.7:p.Ala354Ser
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ENST00000346085.10:c.3085G>T
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ENSP00000344546.5:p.Ala1029Ser
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ENST00000350026.10:c.2797G>T
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ENSP00000055163.7:p.Ala933Ser
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ENST00000414678.7:c.1204G>T
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ENSP00000412835.2:p.Ala402Ser
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ENST00000452544.2:n.947G>T
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ENST00000635849.1:c.367G>T
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ENSP00000490948.1:p.Ala123Ser
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ENST00000635957.1:c.1G>T
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ENSP00000490385.1:p.Ala1Ser
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ENST00000636426.1:n.180G>T
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ENST00000636930.2:c.3046G>T
MANE Select
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ENSP00000490491.2:p.Ala1016Ser
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ENST00000637015.1:c.285G>T
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ENST00000637568.1:c.89G>T
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|
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ENST00000637810.1:c.547G>T
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ENSP00000489636.1:p.Ala183Ser
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ENST00000637904.1:c.547G>T
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ENSP00000490550.1:p.Ala183Ser
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ENST00000647938.1:c.2836G>T
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ENSP00000498155.1:p.Ala946Ser
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ENST00000674190.1:n.1795G>T
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|
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ENST00000319584.10:c.1063G>T
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ENSP00000313006.6:p.Ala355Ser
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ENST00000346085.9:c.2836G>T
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ENSP00000344546.4:p.Ala946Ser
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ENST00000350026.9:c.2797G>T
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ENSP00000055163.7:p.Ala933Ser
|
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ENST00000414678.6:c.1204G>T
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ENSP00000412835.2:p.Ala402Ser
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ENST00000452544.1:n.893G>T
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|
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ENST00000478761.3:c.119G>T
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NM_017519.2:c.2797G>T
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NP_059989.2:p.Ala933Ser
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NM_020732.3:c.2836G>T
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NP_065783.3:p.Ala946Ser
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XM_005267069.3:c.2797G>T
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XP_005267126.2:p.Ala933Ser
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XM_011535984.1:c.1747G>T
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XP_011534286.1:p.Ala583Ser
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XM_011535985.1:c.1567G>T
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XP_011534287.1:p.Ala523Ser
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XM_011535986.1:c.1327G>T
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XP_011534288.1:p.Ala443Ser
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XM_011535987.1:c.946G>T
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XP_011534289.1:p.Ala316Ser
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XM_011535988.1:c.-20+15701G>T
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XP_011534290.1:n.-20+15701G>T
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NM_001346813.1:c.2797G>T
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NP_001333742.1:p.Ala933Ser
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NM_001363725.1:c.547G>T
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NP_001350654.1:p.Ala183Ser
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XM_011535984.2:c.2878G>T
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XP_011534286.2:p.Ala960Ser
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XM_011535988.3:c.-20+15701G>T
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XP_011534290.1:n.-20+15701G>T
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|
XM_017011103.2:c.2878G>T
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XP_016866592.1:p.Ala960Ser
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XM_017011104.1:c.2878G>T
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XP_016866593.1:p.Ala960Ser
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XM_017011105.2:c.2878G>T
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XP_016866594.1:p.Ala960Ser
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|
XM_017011106.2:c.2878G>T
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XP_016866595.1:p.Ala960Ser
|
|
XM_017011107.2:c.2698G>T
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XP_016866596.1:p.Ala900Ser
|
|
XR_002956289.1:n.2961G>T
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|
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NM_001363725.2:c.547G>T
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NP_001350654.1:p.Ala183Ser
|
|
NM_001371656.1:c.3085G>T
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NP_001358585.1:p.Ala1029Ser
|
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NM_001374820.1:c.3085G>T
|
NP_001361749.1:p.Ala1029Ser
|
|
NM_001374828.1:c.3046G>T
MANE Select
|
NP_001361757.1:p.Ala1016Ser
|
|
NM_017519.3:c.3046G>T
|
NP_059989.3:p.Ala1016Ser
|
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