ENST00000682565.1:c.10106T>G
|
ENSP00000507671.1:p.Ile3369Ser
|
|
ENST00000682801.1:c.10106T>G
|
ENSP00000507862.1:p.Ile3369Ser
|
|
ENST00000682859.1:c.10106T>G
|
ENSP00000508222.1:p.Ile3369Ser
|
|
ENST00000683791.1:c.3192T>G
|
|
|
ENST00000684460.1:c.7387T>G
|
|
|
ENST00000684548.1:c.10106T>G
|
ENSP00000507421.1:p.Ile3369Ser
|
|
ENST00000684590.1:c.4553T>G
|
ENSP00000507376.1:p.Ile1518Ser
|
|
ENST00000684656.1:c.7432T>G
|
|
|
ENST00000613296.6:c.10487T>G
MANE Select
|
ENSP00000482968.1:p.Ile3496Ser
|
|
ENST00000651057.1:c.641T>G
|
ENSP00000498504.1:p.Ile214Ser
|
|
ENST00000651434.1:c.1843T>G
|
|
|
ENST00000652487.1:c.1584T>G
|
|
|
ENST00000423048.5:c.3978T>G
|
ENSP00000399833.1:n.3978T>G
|
|
ENST00000484298.5:c.10361T>G
|
ENSP00000478155.1:p.Ile3454Ser
|
|
ENST00000613296.4:c.10487T>G
|
ENSP00000482968.1:p.Ile3496Ser
|
|
ENST00000614410.4:c.10487T>G
|
ENSP00000479094.1:p.Ile3496Ser
|
|
ENST00000620466.4:n.4290T>G
|
|
|
NM_015120.4:c.10490T>G , LRG_741t1:c.10490T>G
|
NP_055935.4:p.Ile3497Ser
|
|
NM_001378454.1:c.10487T>G
MANE Select
|
NP_001365383.1:p.Ile3496Ser
|
|