ENST00000682565.1:c.7416A>T
|
ENSP00000507671.1:p.Arg2472Ser
|
|
ENST00000682801.1:c.7416A>T
|
ENSP00000507862.1:p.Arg2472Ser
|
|
ENST00000682859.1:c.7416A>T
|
ENSP00000508222.1:p.Arg2472Ser
|
|
ENST00000683791.1:c.808A>T
|
|
|
ENST00000684460.1:c.4868A>T
|
|
|
ENST00000684548.1:c.7416A>T
|
ENSP00000507421.1:p.Arg2472Ser
|
|
ENST00000684590.1:c.1863A>T
|
ENSP00000507376.1:p.Arg621Ser
|
|
ENST00000684656.1:c.4868A>T
|
|
|
ENST00000613296.6:c.7797A>T
MANE Select
|
ENSP00000482968.1:p.Arg2599Ser
|
|
ENST00000651434.1:c.896-30019A>T
|
|
|
ENST00000423048.5:c.2628A>T
|
ENSP00000399833.1:p.Arg876Ser
|
|
ENST00000484298.5:c.7671A>T
|
ENSP00000478155.1:p.Arg2557Ser
|
|
ENST00000613296.4:c.7797A>T
|
ENSP00000482968.1:p.Arg2599Ser
|
|
ENST00000614410.4:c.7797A>T
|
ENSP00000479094.1:p.Arg2599Ser
|
|
ENST00000620466.4:n.1600A>T
|
|
|
NM_015120.4:c.7800A>T , LRG_741t1:c.7800A>T
|
NP_055935.4:p.Arg2600Ser
|
|
NM_001378454.1:c.7797A>T
MANE Select
|
NP_001365383.1:p.Arg2599Ser
|
|