ENST00000682565.1:c.10516G>T
|
ENSP00000507671.1:p.Ala3506Ser
|
|
ENST00000682801.1:c.10516G>T
|
ENSP00000507862.1:p.Ala3506Ser
|
|
ENST00000682859.1:c.10516G>T
|
ENSP00000508222.1:p.Ala3506Ser
|
|
ENST00000683791.1:c.3602G>T
|
|
|
ENST00000684460.1:c.7797G>T
|
|
|
ENST00000684548.1:c.10516G>T
|
ENSP00000507421.1:p.Ala3506Ser
|
|
ENST00000684590.1:c.4963G>T
|
ENSP00000507376.1:p.Ala1655Ser
|
|
ENST00000684656.1:c.7842G>T
|
|
|
ENST00000613296.6:c.10897G>T
MANE Select
|
ENSP00000482968.1:p.Ala3633Ser
|
|
ENST00000651057.1:c.1051G>T
|
ENSP00000498504.1:p.Ala351Ser
|
|
ENST00000651434.1:c.2253G>T
|
|
|
ENST00000651750.1:c.285G>T
|
|
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ENST00000652487.1:c.1994G>T
|
|
|
ENST00000423048.5:c.4388G>T
|
ENSP00000399833.1:n.4388G>T
|
|
ENST00000484298.5:c.10771G>T
|
ENSP00000478155.1:p.Ala3591Ser
|
|
ENST00000613296.4:c.10897G>T
|
ENSP00000482968.1:p.Ala3633Ser
|
|
ENST00000614410.4:c.10897G>T
|
ENSP00000479094.1:p.Ala3633Ser
|
|
ENST00000620466.4:n.4700G>T
|
|
|
NM_015120.4:c.10900G>T , LRG_741t1:c.10900G>T
|
NP_055935.4:p.Ala3634Ser
|
|
NM_001378454.1:c.10897G>T
MANE Select
|
NP_001365383.1:p.Ala3633Ser
|
|