ENST00000336411.7:c.1425C>T
|
ENSP00000337915.3:p.Gly475=
|
|
ENST00000651162.1:n.767C>T
|
|
|
ENST00000651514.1:c.1332C>T
MANE Select
|
ENSP00000498939.1:p.Gly444=
|
|
ENST00000651783.1:c.873C>T
|
ENSP00000498924.1:p.Gly291=
|
|
ENST00000652018.1:c.1185C>T
|
ENSP00000498733.1:p.Gly395=
|
|
ENST00000336411.6:c.1332C>T
|
ENSP00000337915.2:p.Gly444=
|
|
ENST00000354593.6:c.882C>T
|
ENSP00000346607.2:p.Gly294=
|
|
NM_001202855.2:c.1329C>T
|
NP_001189784.1:p.Gly443=
|
|
NM_017460.5:c.1332C>T
|
NP_059488.2:p.Gly444=
|
|
XM_011515841.1:c.1425C>T
|
XP_011514143.1:p.Gly475=
|
|
XM_011515842.1:c.1422C>T
|
XP_011514144.1:p.Gly474=
|
|
NM_017460.6:c.1332C>T
MANE Select
|
NP_059488.2:p.Gly444=
|
|
NM_001202855.3:c.1329C>T
|
NP_001189784.1:p.Gly443=
|
|