ENST00000269217.11:c.2894T>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Leu965Trp
|
|
ENST00000313654.14:c.7721T>G
MANE Select
|
ENSP00000324532.8:p.Leu2574Trp
|
|
ENST00000649721.1:c.4316T>G
|
ENSP00000497885.1:p.Leu1439Trp
|
|
ENST00000269217.10:c.2894T>G
|
ENSP00000269217.5:p.Leu965Trp
|
|
ENST00000313654.13:c.7721T>G
|
ENSP00000324532.8:p.Leu2574Trp
|
|
ENST00000399516.7:c.7553T>G
|
ENSP00000382432.2:p.Leu2518Trp
|
|
ENST00000586751.5:c.2499T>G
|
|
|
ENST00000587184.5:c.2726T>G
|
ENSP00000466557.1:p.Leu909Trp
|
|
ENST00000588770.5:n.2299T>G
|
|
|
NM_000227.4:c.2894T>G
|
NP_000218.3:p.Leu965Trp
|
|
NM_001127717.2:c.7553T>G
|
NP_001121189.2:p.Leu2518Trp
|
|
NM_001127718.2:c.2726T>G
|
NP_001121190.2:p.Leu909Trp
|
|
NM_198129.2:c.7721T>G
|
NP_937762.2:p.Leu2574Trp
|
|
XM_011525978.1:c.7748T>G
|
XP_011524280.1:p.Leu2583Trp
|
|
XM_011525979.1:c.7739T>G
|
XP_011524281.1:p.Leu2580Trp
|
|
XM_011525980.1:c.7730T>G
|
XP_011524282.1:p.Leu2577Trp
|
|
XM_011525981.1:c.7616T>G
|
XP_011524283.1:p.Leu2539Trp
|
|
XM_011525982.1:c.7451T>G
|
XP_011524284.1:p.Leu2484Trp
|
|
XM_011525978.2:c.7748T>G
|
XP_011524280.1:p.Leu2583Trp
|
|
XM_011525979.2:c.7739T>G
|
XP_011524281.1:p.Leu2580Trp
|
|
XM_011525980.2:c.7730T>G
|
XP_011524282.1:p.Leu2577Trp
|
|
XM_011525981.2:c.7616T>G
|
XP_011524283.1:p.Leu2539Trp
|
|
XM_011525982.2:c.7451T>G
|
XP_011524284.1:p.Leu2484Trp
|
|
XM_017025743.1:c.5600T>G
|
XP_016881232.1:p.Leu1867Trp
|
|
XM_017025744.1:c.3290T>G
|
XP_016881233.1:p.Leu1097Trp
|
|
XR_001753199.1:n.7989T>G
|
|
|
NM_000227.5:c.2894T>G
|
NP_000218.3:p.Leu965Trp
|
|
NM_001127717.3:c.7553T>G
|
NP_001121189.2:p.Leu2518Trp
|
|
NM_001127718.3:c.2726T>G
|
NP_001121190.2:p.Leu909Trp
|
|
NM_198129.3:c.7721T>G
|
NP_937762.2:p.Leu2574Trp
|
|
NM_000227.6:c.2894T>G
MANE Plus Clinical
|
NP_000218.3:p.Leu965Trp
|
|
NM_001127717.4:c.7553T>G
|
NP_001121189.2:p.Leu2518Trp
|
|
NM_001127718.4:c.2726T>G
|
NP_001121190.2:p.Leu909Trp
|
|
NM_198129.4:c.7721T>G
MANE Select
|
NP_937762.2:p.Leu2574Trp
|
|