ENST00000682565.1:c.7337T>G
|
ENSP00000507671.1:p.Val2446Gly
|
|
ENST00000682801.1:c.7337T>G
|
ENSP00000507862.1:p.Val2446Gly
|
|
ENST00000682859.1:c.7337T>G
|
ENSP00000508222.1:p.Val2446Gly
|
|
ENST00000683791.1:c.729T>G
|
|
|
ENST00000684460.1:c.4789T>G
|
|
|
ENST00000684548.1:c.7337T>G
|
ENSP00000507421.1:p.Val2446Gly
|
|
ENST00000684590.1:c.1784T>G
|
ENSP00000507376.1:p.Val595Gly
|
|
ENST00000684656.1:c.4789T>G
|
|
|
ENST00000613296.6:c.7718T>G
MANE Select
|
ENSP00000482968.1:p.Val2573Gly
|
|
ENST00000651434.1:c.896-30098T>G
|
|
|
ENST00000423048.5:c.2549T>G
|
ENSP00000399833.1:p.Val850Gly
|
|
ENST00000484298.5:c.7592T>G
|
ENSP00000478155.1:p.Val2531Gly
|
|
ENST00000613296.4:c.7718T>G
|
ENSP00000482968.1:p.Val2573Gly
|
|
ENST00000614410.4:c.7718T>G
|
ENSP00000479094.1:p.Val2573Gly
|
|
ENST00000620466.4:n.1521T>G
|
|
|
NM_015120.4:c.7721T>G , LRG_741t1:c.7721T>G
|
NP_055935.4:p.Val2574Gly
|
|
NM_001378454.1:c.7718T>G
MANE Select
|
NP_001365383.1:p.Val2573Gly
|
|