ENST00000336411.7:c.659T=
|
ENSP00000337915.3:p.Phe220=
|
|
ENST00000651514.1:c.659T=
MANE Select
|
ENSP00000498939.1:p.Phe220=
|
|
ENST00000651783.1:c.200T=
|
ENSP00000498924.1:p.Phe67=
|
|
ENST00000652018.1:c.512T=
|
ENSP00000498733.1:p.Phe171=
|
|
ENST00000336411.6:c.659T=
|
ENSP00000337915.2:p.Phe220=
|
|
ENST00000354593.6:c.209T=
|
ENSP00000346607.2:p.Phe70=
|
|
NM_001202855.2:c.659T=
|
NP_001189784.1:p.Phe220=
|
|
NM_017460.5:c.659T=
|
NP_059488.2:p.Phe220=
|
|
XM_011515841.1:c.659T=
|
XP_011514143.1:p.Phe220=
|
|
XM_011515842.1:c.659T=
|
XP_011514144.1:p.Phe220=
|
|
NM_017460.6:c.659T=
MANE Select
|
NP_059488.2:p.Phe220=
|
|
NM_001202855.3:c.659T=
|
NP_001189784.1:p.Phe220=
|
|