ENST00000375708.4:c.2694G>C
MANE Select
|
ENSP00000364860.3:p.Gln898His
|
|
ENST00000375708.3:c.2694G>C
|
ENSP00000364860.3:p.Gln898His
|
|
ENST00000375715.5:c.1920+354G>C
|
ENSP00000364867.1:n.1920+354G>C
|
|
ENST00000550066.5:n.3162G>C
|
|
|
NM_004560.3:c.2694G>C
|
NP_004551.2:p.Gln898His
|
|
XM_005252008.3:c.2274G>C
|
XP_005252065.1:p.Gln758His
|
|
XM_005252009.3:c.1491G>C
|
XP_005252066.1:p.Gln497His
|
|
XM_006717121.2:c.2274G>C
|
XP_006717184.1:p.Gln758His
|
|
XM_011518721.1:c.2274G>C
|
XP_011517023.1:p.Gln758His
|
|
XM_005252008.4:c.2274G>C
|
XP_005252065.1:p.Gln758His
|
|
XM_006717121.3:c.2274G>C
|
XP_006717184.1:p.Gln758His
|
|
XM_017014762.1:c.2685G>C
|
XP_016870251.1:p.Gln895His
|
|
XM_017014763.1:c.2274G>C
|
XP_016870252.1:p.Gln758His
|
|
NM_004560.4:c.2694G>C
MANE Select
|
NP_004551.2:p.Gln898His
|
|