ENST00000682565.1:c.7426G>T
|
ENSP00000507671.1:p.Ala2476Ser
|
|
ENST00000682801.1:c.7426G>T
|
ENSP00000507862.1:p.Ala2476Ser
|
|
ENST00000682859.1:c.7426G>T
|
ENSP00000508222.1:p.Ala2476Ser
|
|
ENST00000683791.1:c.818G>T
|
|
|
ENST00000684460.1:c.4878G>T
|
|
|
ENST00000684548.1:c.7426G>T
|
ENSP00000507421.1:p.Ala2476Ser
|
|
ENST00000684590.1:c.1873G>T
|
ENSP00000507376.1:p.Ala625Ser
|
|
ENST00000684656.1:c.4878G>T
|
|
|
ENST00000613296.6:c.7807G>T
MANE Select
|
ENSP00000482968.1:p.Ala2603Ser
|
|
ENST00000651434.1:c.896-30009G>T
|
|
|
ENST00000423048.5:c.2638G>T
|
ENSP00000399833.1:p.Ala880Ser
|
|
ENST00000484298.5:c.7681G>T
|
ENSP00000478155.1:p.Ala2561Ser
|
|
ENST00000613296.4:c.7807G>T
|
ENSP00000482968.1:p.Ala2603Ser
|
|
ENST00000614410.4:c.7807G>T
|
ENSP00000479094.1:p.Ala2603Ser
|
|
ENST00000620466.4:n.1610G>T
|
|
|
NM_015120.4:c.7810G>T , LRG_741t1:c.7810G>T
|
NP_055935.4:p.Ala2604Ser
|
|
NM_001378454.1:c.7807G>T
MANE Select
|
NP_001365383.1:p.Ala2603Ser
|
|