ENST00000262461.7:c.3582A>G
MANE Select
|
ENSP00000262461.2:p.Leu1194=
|
|
ENST00000262461.6:c.3582A>G
|
ENSP00000262461.2:p.Leu1194=
|
|
ENST00000343225.4:c.3534A>G
|
ENSP00000340878.4:p.Leu1178=
|
|
ENST00000509205.5:c.*195A>G
|
ENSP00000427109.1:n.*195A>G
|
|
NM_001046.2:c.3582A>G
|
NP_001037.1:p.Leu1194=
|
|
NM_001256461.1:c.3534A>G
|
NP_001243390.1:p.Leu1178=
|
|
NR_046207.1:n.3812A>G
|
|
|
XM_017009771.1:c.1824A>G
|
XP_016865260.1:p.Leu608=
|
|
XR_001742214.1:n.3806A>G
|
|
|
NM_001046.3:c.3582A>G
MANE Select
|
NP_001037.1:p.Leu1194=
|
|
NM_001256461.2:c.3534A>G
|
NP_001243390.1:p.Leu1178=
|
|
NR_046207.2:n.3837A>G
|
|
|