ENST00000336411.7:c.1467A>C
|
ENSP00000337915.3:p.Arg489Ser
|
|
ENST00000651162.1:n.809A>C
|
|
|
ENST00000651514.1:c.1374A>C
MANE Select
|
ENSP00000498939.1:p.Arg458Ser
|
|
ENST00000651783.1:c.915A>C
|
ENSP00000498924.1:p.Arg305Ser
|
|
ENST00000652018.1:c.1227A>C
|
ENSP00000498733.1:p.Arg409Ser
|
|
ENST00000336411.6:c.1374A>C
|
ENSP00000337915.2:p.Arg458Ser
|
|
ENST00000354593.6:c.924A>C
|
ENSP00000346607.2:p.Arg308Ser
|
|
NM_001202855.2:c.1371A>C
|
NP_001189784.1:p.Arg457Ser
|
|
NM_017460.5:c.1374A>C
|
NP_059488.2:p.Arg458Ser
|
|
XM_011515841.1:c.1467A>C
|
XP_011514143.1:p.Arg489Ser
|
|
XM_011515842.1:c.1464A>C
|
XP_011514144.1:p.Arg488Ser
|
|
NM_017460.6:c.1374A>C
MANE Select
|
NP_059488.2:p.Arg458Ser
|
|
NM_001202855.3:c.1371A>C
|
NP_001189784.1:p.Arg457Ser
|
|