ENST00000295408.9:c.641T>G
MANE Select
|
ENSP00000295408.4:p.Phe214Cys
|
|
ENST00000295408.8:c.641T>G
|
ENSP00000295408.4:p.Phe214Cys
|
|
ENST00000409780.5:c.113T>G
|
ENSP00000387277.1:p.Phe38Cys
|
|
ENST00000421804.6:c.641T>G
|
ENSP00000389152.2:p.Phe214Cys
|
|
ENST00000439966.5:c.*114T>G
|
ENSP00000402129.1:n.*114T>G
|
|
ENST00000616902.4:c.-575T>G
|
ENSP00000482824.1:n.-575T>G
|
|
NM_006343.2:c.641T>G
|
NP_006334.2:p.Phe214Cys
|
|
XM_005263565.3:c.641T>G
|
XP_005263622.1:p.Phe214Cys
|
|
XM_005263568.3:c.641T>G
|
XP_005263625.1:p.Phe214Cys
|
|
XM_011510490.1:c.452T>G
|
XP_011508792.1:p.Phe151Cys
|
|
XM_005263565.4:c.641T>G
|
XP_005263622.1:p.Phe214Cys
|
|
XM_005263568.4:c.641T>G
|
XP_005263625.1:p.Phe214Cys
|
|
XM_011510490.3:c.452T>G
|
XP_011508792.1:p.Phe151Cys
|
|
XM_017003164.1:c.452T>G
|
XP_016858653.1:p.Phe151Cys
|
|
XM_017003165.2:c.-627T>G
|
XP_016858654.1:n.-627T>G
|
|
NM_006343.3:c.641T>G
MANE Select
|
NP_006334.2:p.Phe214Cys
|
|