ENST00000295408.9:c.1531G>A
MANE Select
|
ENSP00000295408.4:p.Gly511Arg
|
|
ENST00000295408.8:c.1531G>A
|
ENSP00000295408.4:p.Gly511Arg
|
|
ENST00000409780.5:c.1003G>A
|
ENSP00000387277.1:p.Gly335Arg
|
|
ENST00000421804.6:c.1531G>A
|
ENSP00000389152.2:p.Gly511Arg
|
|
ENST00000439966.5:c.*1004G>A
|
ENSP00000402129.1:n.*1004G>A
|
|
ENST00000473065.1:n.34G>A
|
|
|
ENST00000616902.4:c.500G>A
|
ENSP00000482824.1:p.Trp167Ter
|
|
NM_006343.2:c.1531G>A
|
NP_006334.2:p.Gly511Arg
|
|
XM_005263565.3:c.1531G>A
|
XP_005263622.1:p.Gly511Arg
|
|
XM_005263568.3:c.1531G>A
|
XP_005263625.1:p.Gly511Arg
|
|
XM_011510490.1:c.1342G>A
|
XP_011508792.1:p.Gly448Arg
|
|
XM_011510491.1:c.316G>A
|
XP_011508793.1:p.Gly106Arg
|
|
XM_005263565.4:c.1531G>A
|
XP_005263622.1:p.Gly511Arg
|
|
XM_005263568.4:c.1531G>A
|
XP_005263625.1:p.Gly511Arg
|
|
XM_011510490.3:c.1342G>A
|
XP_011508792.1:p.Gly448Arg
|
|
XM_017003164.1:c.1342G>A
|
XP_016858653.1:p.Gly448Arg
|
|
XM_017003165.2:c.316G>A
|
XP_016858654.1:p.Gly106Arg
|
|
NM_006343.3:c.1531G>A
MANE Select
|
NP_006334.2:p.Gly511Arg
|
|