ENST00000375708.4:c.1385A>G
MANE Select
|
ENSP00000364860.3:p.Gln462Arg
|
|
ENST00000375708.3:c.1385A>G
|
ENSP00000364860.3:p.Gln462Arg
|
|
ENST00000375715.5:c.965A>G
|
ENSP00000364867.1:p.Gln322Arg
|
|
ENST00000550066.5:n.1853A>G
|
|
|
NM_004560.3:c.1385A>G
|
NP_004551.2:p.Gln462Arg
|
|
XM_005252008.3:c.965A>G
|
XP_005252065.1:p.Gln322Arg
|
|
XM_005252009.3:c.182A>G
|
XP_005252066.1:p.Gln61Arg
|
|
XM_006717121.2:c.965A>G
|
XP_006717184.1:p.Gln322Arg
|
|
XM_011518721.1:c.965A>G
|
XP_011517023.1:p.Gln322Arg
|
|
NM_001318204.1:c.*52A>G
|
NP_001305133.1:n.*52A>G
|
|
XM_005252008.4:c.965A>G
|
XP_005252065.1:p.Gln322Arg
|
|
XM_006717121.3:c.965A>G
|
XP_006717184.1:p.Gln322Arg
|
|
XM_017014762.1:c.1376A>G
|
XP_016870251.1:p.Gln459Arg
|
|
XM_017014763.1:c.965A>G
|
XP_016870252.1:p.Gln322Arg
|
|
XR_001746315.1:n.1594A>G
|
|
|
NM_004560.4:c.1385A>G
MANE Select
|
NP_004551.2:p.Gln462Arg
|
|
NM_001318204.2:c.*52A>G
|
NP_001305133.1:n.*52A>G
|
|