ENST00000559133.6:c.6535G>A
|
ENSP00000453958.2:p.Gly2179Arg
|
|
ENST00000674301.2:c.6535G>A
|
ENSP00000501333.2:p.Gly2179Arg
|
|
ENST00000682170.1:n.144G>A
|
|
|
ENST00000316623.10:c.6535G>A
MANE Select
|
ENSP00000325527.5:p.Gly2179Arg
|
|
ENST00000674301.1:c.1534G>A
|
ENSP00000501333.1:p.Gly512Arg
|
|
ENST00000316623.9:c.6535G>A
|
ENSP00000325527.5:p.Gly2179Arg
|
|
ENST00000537463.6:c.*2298G>A
|
ENSP00000440294.2:n.*2298G>A
|
|
ENST00000559133.5:c.1842G>A
|
|
|
NM_000138.4:c.6535G>A , LRG_778t1:c.6535G>A
|
NP_000129.3:p.Gly2179Arg
|
|
NM_000138.5:c.6535G>A
MANE Select
|
NP_000129.3:p.Gly2179Arg
|
|