ENST00000559133.6:c.6862G>C
|
ENSP00000453958.2:p.Gly2288Arg
|
|
ENST00000674301.2:c.*313G>C
|
ENSP00000501333.2:n.*313G>C
|
|
ENST00000682170.1:n.471G>C
|
|
|
ENST00000316623.10:c.6862G>C
MANE Select
|
ENSP00000325527.5:p.Gly2288Arg
|
|
ENST00000674301.1:c.1966G>C
|
ENSP00000501333.1:n.1966G>C
|
|
ENST00000316623.9:c.6862G>C
|
ENSP00000325527.5:p.Gly2288Arg
|
|
ENST00000559133.5:c.2169G>C
|
|
|
ENST00000560720.1:n.149G>C
|
|
|
NM_000138.4:c.6862G>C , LRG_778t1:c.6862G>C
|
NP_000129.3:p.Gly2288Arg
|
|
NM_000138.5:c.6862G>C
MANE Select
|
NP_000129.3:p.Gly2288Arg
|
|