ENST00000570803.6:c.2511C>T
|
ENSP00000460543.2:p.Arg837=
|
|
ENST00000572080.2:c.*649C>T
|
ENSP00000459972.2:n.*649C>T
|
|
ENST00000577106.6:c.2511C>T
|
ENSP00000458306.2:p.Arg837=
|
|
ENST00000302262.8:c.2511C>T
MANE Select
|
ENSP00000305692.3:p.Arg837=
|
|
ENST00000302262.7:c.2511C>T
|
ENSP00000305692.3:p.Arg837=
|
|
ENST00000390015.7:c.2511C>T
|
ENSP00000374665.3:p.Arg837=
|
|
ENST00000573556.1:n.464C>T
|
|
|
NM_000152.3:c.2511C>T , LRG_673t1:c.2511C>T
|
NP_000143.2:p.Arg837=
|
|
NM_001079803.1:c.2511C>T
|
NP_001073271.1:p.Arg837=
|
|
NM_001079804.1:c.2511C>T
|
NP_001073272.1:p.Arg837=
|
|
XM_005257193.1:c.2511C>T
|
XP_005257250.1:p.Arg837=
|
|
XM_005257194.3:c.2511C>T
|
XP_005257251.1:p.Arg837=
|
|
NM_000152.4:c.2511C>T
|
NP_000143.2:p.Arg837=
|
|
NM_001079803.2:c.2511C>T
|
NP_001073271.1:p.Arg837=
|
|
NM_001079804.2:c.2511C>T
|
NP_001073272.1:p.Arg837=
|
|
XM_005257193.2:c.2511C>T
|
XP_005257250.1:p.Arg837=
|
|
XM_005257194.4:c.2511C>T
|
XP_005257251.1:p.Arg837=
|
|
NM_000152.5:c.2511C>T
MANE Select
|
NP_000143.2:p.Arg837=
|
|
NM_001079803.3:c.2511C>T
|
NP_001073271.1:p.Arg837=
|
|
NM_001079804.3:c.2511C>T
|
NP_001073272.1:p.Arg837=
|
|