ENST00000559133.6:c.5816G>T
|
ENSP00000453958.2:p.Gly1939Val
|
|
ENST00000674301.2:c.5816G>T
|
ENSP00000501333.2:p.Gly1939Val
|
|
ENST00000684448.1:n.4490G>T
|
|
|
ENST00000316623.10:c.5816G>T
MANE Select
|
ENSP00000325527.5:p.Gly1939Val
|
|
ENST00000674301.1:c.815G>T
|
ENSP00000501333.1:p.Gly272Val
|
|
ENST00000316623.9:c.5816G>T
|
ENSP00000325527.5:p.Gly1939Val
|
|
ENST00000537463.6:c.*1579G>T
|
ENSP00000440294.2:n.*1579G>T
|
|
ENST00000559133.5:c.1123G>T
|
|
|
NM_000138.4:c.5816G>T , LRG_778t1:c.5816G>T
|
NP_000129.3:p.Gly1939Val
|
|
NM_000138.5:c.5816G>T
MANE Select
|
NP_000129.3:p.Gly1939Val
|
|