ENST00000269217.11:c.4696T>C
MANE Plus Clinical
|
ENSP00000269217.5:p.Leu1566=
|
|
ENST00000313654.14:c.9523T>C
MANE Select
|
ENSP00000324532.8:p.Leu3175=
|
|
ENST00000649721.1:c.6118T>C
|
ENSP00000497885.1:p.Leu2040=
|
|
ENST00000269217.10:c.4696T>C
|
ENSP00000269217.5:p.Leu1566=
|
|
ENST00000313654.13:c.9523T>C
|
ENSP00000324532.8:p.Leu3175=
|
|
ENST00000399516.7:c.9355T>C
|
ENSP00000382432.2:p.Leu3119=
|
|
ENST00000587184.5:c.4528T>C
|
ENSP00000466557.1:p.Leu1510=
|
|
ENST00000588004.1:c.44T>C
|
|
|
ENST00000588770.5:n.4101T>C
|
|
|
NM_000227.4:c.4696T>C
|
NP_000218.3:p.Leu1566=
|
|
NM_001127717.2:c.9355T>C
|
NP_001121189.2:p.Leu3119=
|
|
NM_001127718.2:c.4528T>C
|
NP_001121190.2:p.Leu1510=
|
|
NM_198129.2:c.9523T>C
|
NP_937762.2:p.Leu3175=
|
|
XM_011525978.1:c.9550T>C
|
XP_011524280.1:p.Leu3184=
|
|
XM_011525979.1:c.9541T>C
|
XP_011524281.1:p.Leu3181=
|
|
XM_011525980.1:c.9532T>C
|
XP_011524282.1:p.Leu3178=
|
|
XM_011525981.1:c.9418T>C
|
XP_011524283.1:p.Leu3140=
|
|
XM_011525982.1:c.9253T>C
|
XP_011524284.1:p.Leu3085=
|
|
XM_011525978.2:c.9550T>C
|
XP_011524280.1:p.Leu3184=
|
|
XM_011525979.2:c.9541T>C
|
XP_011524281.1:p.Leu3181=
|
|
XM_011525980.2:c.9532T>C
|
XP_011524282.1:p.Leu3178=
|
|
XM_011525981.2:c.9418T>C
|
XP_011524283.1:p.Leu3140=
|
|
XM_011525982.2:c.9253T>C
|
XP_011524284.1:p.Leu3085=
|
|
XM_017025743.1:c.7402T>C
|
XP_016881232.1:p.Leu2468=
|
|
XM_017025744.1:c.5092T>C
|
XP_016881233.1:p.Leu1698=
|
|
XR_001753199.1:n.9791T>C
|
|
|
NM_000227.5:c.4696T>C
|
NP_000218.3:p.Leu1566=
|
|
NM_001127717.3:c.9355T>C
|
NP_001121189.2:p.Leu3119=
|
|
NM_001127718.3:c.4528T>C
|
NP_001121190.2:p.Leu1510=
|
|
NM_198129.3:c.9523T>C
|
NP_937762.2:p.Leu3175=
|
|
NM_000227.6:c.4696T>C
MANE Plus Clinical
|
NP_000218.3:p.Leu1566=
|
|
NM_001127717.4:c.9355T>C
|
NP_001121189.2:p.Leu3119=
|
|
NM_001127718.4:c.4528T>C
|
NP_001121190.2:p.Leu1510=
|
|
NM_198129.4:c.9523T>C
MANE Select
|
NP_937762.2:p.Leu3175=
|
|