ENST00000350026.11:c.2900G>C
|
ENSP00000055163.8:p.Gly967Ala
|
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ENST00000414678.8:c.2810G>C
|
ENSP00000412835.3:p.Gly937Ala
|
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ENST00000637015.2:c.2900G>C
|
ENSP00000489729.2:p.Gly967Ala
|
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ENST00000319584.11:c.914G>C
|
ENSP00000313006.7:p.Gly305Ala
|
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ENST00000346085.10:c.2939G>C
|
ENSP00000344546.5:p.Gly980Ala
|
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ENST00000350026.10:c.2651G>C
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ENSP00000055163.7:p.Gly884Ala
|
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ENST00000414678.7:c.1058G>C
|
ENSP00000412835.2:p.Gly353Ala
|
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ENST00000452544.2:n.801G>C
|
|
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ENST00000635849.1:c.221G>C
|
ENSP00000490948.1:p.Gly74Ala
|
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ENST00000636426.1:n.34G>C
|
|
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ENST00000636930.2:c.2900G>C
MANE Select
|
ENSP00000490491.2:p.Gly967Ala
|
|
ENST00000637015.1:c.139G>C
|
|
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ENST00000637810.1:c.401G>C
|
ENSP00000489636.1:p.Gly134Ala
|
|
ENST00000637904.1:c.401G>C
|
ENSP00000490550.1:p.Gly134Ala
|
|
ENST00000647938.1:c.2690G>C
|
ENSP00000498155.1:p.Gly897Ala
|
|
ENST00000674190.1:n.1649G>C
|
|
|
ENST00000319584.10:c.917G>C
|
ENSP00000313006.6:p.Gly306Ala
|
|
ENST00000346085.9:c.2690G>C
|
ENSP00000344546.4:p.Gly897Ala
|
|
ENST00000350026.9:c.2651G>C
|
ENSP00000055163.7:p.Gly884Ala
|
|
ENST00000414678.6:c.1058G>C
|
ENSP00000412835.2:p.Gly353Ala
|
|
ENST00000452544.1:n.747G>C
|
|
|
NM_017519.2:c.2651G>C
|
NP_059989.2:p.Gly884Ala
|
|
NM_020732.3:c.2690G>C
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NP_065783.3:p.Gly897Ala
|
|
XM_005267069.3:c.2651G>C
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XP_005267126.2:p.Gly884Ala
|
|
XM_011535984.1:c.1601G>C
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XP_011534286.1:p.Gly534Ala
|
|
XM_011535985.1:c.1421G>C
|
XP_011534287.1:p.Gly474Ala
|
|
XM_011535986.1:c.1181G>C
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XP_011534288.1:p.Gly394Ala
|
|
XM_011535987.1:c.800G>C
|
XP_011534289.1:p.Gly267Ala
|
|
XM_011535988.1:c.-20+15555G>C
|
XP_011534290.1:n.-20+15555G>C
|
|
NM_001346813.1:c.2651G>C
|
NP_001333742.1:p.Gly884Ala
|
|
NM_001363725.1:c.401G>C
|
NP_001350654.1:p.Gly134Ala
|
|
XM_011535984.2:c.2732G>C
|
XP_011534286.2:p.Gly911Ala
|
|
XM_011535988.3:c.-20+15555G>C
|
XP_011534290.1:n.-20+15555G>C
|
|
XM_017011103.2:c.2732G>C
|
XP_016866592.1:p.Gly911Ala
|
|
XM_017011104.1:c.2732G>C
|
XP_016866593.1:p.Gly911Ala
|
|
XM_017011105.2:c.2732G>C
|
XP_016866594.1:p.Gly911Ala
|
|
XM_017011106.2:c.2732G>C
|
XP_016866595.1:p.Gly911Ala
|
|
XM_017011107.2:c.2552G>C
|
XP_016866596.1:p.Gly851Ala
|
|
XR_002956289.1:n.2815G>C
|
|
|
NM_001363725.2:c.401G>C
|
NP_001350654.1:p.Gly134Ala
|
|
NM_001371656.1:c.2939G>C
|
NP_001358585.1:p.Gly980Ala
|
|
NM_001374820.1:c.2939G>C
|
NP_001361749.1:p.Gly980Ala
|
|
NM_001374828.1:c.2900G>C
MANE Select
|
NP_001361757.1:p.Gly967Ala
|
|
NM_017519.3:c.2900G>C
|
NP_059989.3:p.Gly967Ala
|
|