ENST00000336411.7:c.1482C>T
|
ENSP00000337915.3:p.Phe494=
|
|
ENST00000651162.1:n.824C>T
|
|
|
ENST00000651514.1:c.1389C>T
MANE Select
|
ENSP00000498939.1:p.Phe463=
|
|
ENST00000651783.1:c.930C>T
|
ENSP00000498924.1:p.Phe310=
|
|
ENST00000652018.1:c.1242C>T
|
ENSP00000498733.1:p.Phe414=
|
|
ENST00000336411.6:c.1389C>T
|
ENSP00000337915.2:p.Phe463=
|
|
ENST00000354593.6:c.939C>T
|
ENSP00000346607.2:p.Phe313=
|
|
NM_001202855.2:c.1386C>T
|
NP_001189784.1:p.Phe462=
|
|
NM_017460.5:c.1389C>T
|
NP_059488.2:p.Phe463=
|
|
XM_011515841.1:c.1482C>T
|
XP_011514143.1:p.Phe494=
|
|
XM_011515842.1:c.1479C>T
|
XP_011514144.1:p.Phe493=
|
|
NM_017460.6:c.1389C>T
MANE Select
|
NP_059488.2:p.Phe463=
|
|
NM_001202855.3:c.1386C>T
|
NP_001189784.1:p.Phe462=
|
|