ENST00000295408.9:c.1555T>C
MANE Select
|
ENSP00000295408.4:p.Leu519=
|
|
ENST00000295408.8:c.1555T>C
|
ENSP00000295408.4:p.Leu519=
|
|
ENST00000409780.5:c.1027T>C
|
ENSP00000387277.1:p.Leu343=
|
|
ENST00000421804.6:c.1555T>C
|
ENSP00000389152.2:p.Leu519=
|
|
ENST00000439966.5:c.*1028T>C
|
ENSP00000402129.1:n.*1028T>C
|
|
ENST00000473065.1:n.58T>C
|
|
|
ENST00000616902.4:c.520T>C
|
ENSP00000482824.1:p.Leu174=
|
|
NM_006343.2:c.1555T>C
|
NP_006334.2:p.Leu519=
|
|
XM_005263565.3:c.1555T>C
|
XP_005263622.1:p.Leu519=
|
|
XM_005263568.3:c.1555T>C
|
XP_005263625.1:p.Leu519=
|
|
XM_011510490.1:c.1366T>C
|
XP_011508792.1:p.Leu456=
|
|
XM_011510491.1:c.340T>C
|
XP_011508793.1:p.Leu114=
|
|
XM_005263565.4:c.1555T>C
|
XP_005263622.1:p.Leu519=
|
|
XM_005263568.4:c.1555T>C
|
XP_005263625.1:p.Leu519=
|
|
XM_011510490.3:c.1366T>C
|
XP_011508792.1:p.Leu456=
|
|
XM_017003164.1:c.1366T>C
|
XP_016858653.1:p.Leu456=
|
|
XM_017003165.2:c.340T>C
|
XP_016858654.1:p.Leu114=
|
|
NM_006343.3:c.1555T>C
MANE Select
|
NP_006334.2:p.Leu519=
|
|