ENST00000350026.11:c.3885A>C
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ENSP00000055163.8:p.Pro1295=
|
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ENST00000414678.8:c.3954A>C
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ENSP00000412835.3:p.Pro1318=
|
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ENST00000637015.2:c.4173A>C
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ENSP00000489729.2:p.Pro1391=
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ENST00000346085.10:c.3924A>C
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ENSP00000344546.5:p.Pro1308=
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ENST00000350026.10:c.3636A>C
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ENSP00000055163.7:p.Pro1212=
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ENST00000414678.7:c.2202A>C
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ENSP00000412835.2:p.Pro734=
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ENST00000635849.1:c.1365A>C
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ENSP00000490948.1:p.Pro455=
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ENST00000635957.1:c.999A>C
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ENSP00000490385.1:p.Pro333=
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ENST00000636930.2:c.4044A>C
MANE Select
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ENSP00000490491.2:p.Pro1348=
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ENST00000636940.1:n.2041A>C
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ENST00000637015.1:c.1412A>C
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ENST00000637568.1:c.1326A>C
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ENST00000637741.1:n.710A>C
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ENST00000637810.1:c.1386A>C
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ENSP00000489636.1:p.Pro462=
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ENST00000637904.1:c.1545A>C
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ENSP00000490550.1:p.Pro515=
|
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ENST00000647938.1:c.3675A>C
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ENSP00000498155.1:p.Pro1225=
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ENST00000346085.9:c.3675A>C
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ENSP00000344546.4:p.Pro1225=
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ENST00000350026.9:c.3636A>C
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ENSP00000055163.7:p.Pro1212=
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ENST00000414678.6:c.2202A>C
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ENSP00000412835.2:p.Pro734=
|
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NM_017519.2:c.3636A>C
|
NP_059989.2:p.Pro1212=
|
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NM_020732.3:c.3675A>C
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NP_065783.3:p.Pro1225=
|
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XM_005267069.3:c.3795A>C
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XP_005267126.2:p.Pro1265=
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XM_011535984.1:c.2874A>C
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XP_011534286.1:p.Pro958=
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XM_011535985.1:c.2694A>C
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XP_011534287.1:p.Pro898=
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XM_011535986.1:c.2454A>C
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XP_011534288.1:p.Pro818=
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XM_011535987.1:c.2073A>C
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XP_011534289.1:p.Pro691=
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XM_011535988.1:c.936A>C
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XP_011534290.1:p.Pro312=
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NM_001346813.1:c.3795A>C
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NP_001333742.1:p.Pro1265=
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NM_001363725.1:c.1545A>C
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NP_001350654.1:p.Pro515=
|
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XM_011535984.2:c.4005A>C
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XP_011534286.2:p.Pro1335=
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XM_011535988.3:c.936A>C
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XP_011534290.1:p.Pro312=
|
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XM_017011103.2:c.3906A>C
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XP_016866592.1:p.Pro1302=
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XM_017011104.1:c.3876A>C
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XP_016866593.1:p.Pro1292=
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XM_017011105.2:c.3846A>C
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XP_016866594.1:p.Pro1282=
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XM_017011106.2:c.3717A>C
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XP_016866595.1:p.Pro1239=
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XM_017011107.2:c.3696A>C
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XP_016866596.1:p.Pro1232=
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XR_002956289.1:n.4088A>C
|
|
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NM_001363725.2:c.1545A>C
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NP_001350654.1:p.Pro515=
|
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NM_001371656.1:c.3924A>C
|
NP_001358585.1:p.Pro1308=
|
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NM_001374820.1:c.3924A>C
|
NP_001361749.1:p.Pro1308=
|
|
NM_001374828.1:c.4044A>C
MANE Select
|
NP_001361757.1:p.Pro1348=
|
|
NM_017519.3:c.3885A>C
|
NP_059989.3:p.Pro1295=
|
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