ENST00000307998.11:c.825G>C
MANE Select
|
ENSP00000309953.6:p.Leu275=
|
|
ENST00000307998.10:c.825G>C
|
ENSP00000309953.6:p.Leu275=
|
|
ENST00000526628.5:n.1391G>C
|
|
|
ENST00000527969.1:n.1510G>C
|
|
|
ENST00000528176.5:c.825G>C
|
ENSP00000434151.1:p.Leu275=
|
|
ENST00000530806.5:c.-174G>C
|
ENSP00000436526.1:n.-174G>C
|
|
ENST00000531005.5:n.1819G>C
|
|
|
ENST00000531972.5:c.825G>C
|
ENSP00000435295.1:p.Leu275=
|
|
ENST00000532084.5:n.251G>C
|
|
|
NM_016938.4:c.825G>C
|
NP_058634.4:p.Leu275=
|
|
NR_037718.1:n.1084G>C
|
|
|
NM_016938.5:c.825G>C
MANE Select
|
NP_058634.4:p.Leu275=
|
|
NR_037718.2:n.950G>C
|
|
|