ENST00000682565.1:c.10471G>A
|
ENSP00000507671.1:p.Gly3491Ser
|
|
ENST00000682801.1:c.10471G>A
|
ENSP00000507862.1:p.Gly3491Ser
|
|
ENST00000682859.1:c.10471G>A
|
ENSP00000508222.1:p.Gly3491Ser
|
|
ENST00000683791.1:c.3557G>A
|
|
|
ENST00000684460.1:c.7752G>A
|
|
|
ENST00000684548.1:c.10471G>A
|
ENSP00000507421.1:p.Gly3491Ser
|
|
ENST00000684590.1:c.4918G>A
|
ENSP00000507376.1:p.Gly1640Ser
|
|
ENST00000684656.1:c.7797G>A
|
|
|
ENST00000613296.6:c.10852G>A
MANE Select
|
ENSP00000482968.1:p.Gly3618Ser
|
|
ENST00000651057.1:c.1006G>A
|
ENSP00000498504.1:p.Gly336Ser
|
|
ENST00000651434.1:c.2208G>A
|
|
|
ENST00000651750.1:c.240G>A
|
|
|
ENST00000652487.1:c.1949G>A
|
|
|
ENST00000423048.5:c.4343G>A
|
ENSP00000399833.1:n.4343G>A
|
|
ENST00000484298.5:c.10726G>A
|
ENSP00000478155.1:p.Gly3576Ser
|
|
ENST00000613296.4:c.10852G>A
|
ENSP00000482968.1:p.Gly3618Ser
|
|
ENST00000614410.4:c.10852G>A
|
ENSP00000479094.1:p.Gly3618Ser
|
|
ENST00000620466.4:n.4655G>A
|
|
|
NM_015120.4:c.10855G>A , LRG_741t1:c.10855G>A
|
NP_055935.4:p.Gly3619Ser
|
|
NM_001378454.1:c.10852G>A
MANE Select
|
NP_001365383.1:p.Gly3618Ser
|
|