ENST00000375708.4:c.2718G>T
MANE Select
|
ENSP00000364860.3:p.Gln906His
|
|
ENST00000375708.3:c.2718G>T
|
ENSP00000364860.3:p.Gln906His
|
|
ENST00000375715.5:c.1920+378G>T
|
ENSP00000364867.1:n.1920+378G>T
|
|
ENST00000550066.5:n.3186G>T
|
|
|
NM_004560.3:c.2718G>T
|
NP_004551.2:p.Gln906His
|
|
XM_005252008.3:c.2298G>T
|
XP_005252065.1:p.Gln766His
|
|
XM_005252009.3:c.1515G>T
|
XP_005252066.1:p.Gln505His
|
|
XM_006717121.2:c.2298G>T
|
XP_006717184.1:p.Gln766His
|
|
XM_011518721.1:c.2298G>T
|
XP_011517023.1:p.Gln766His
|
|
XM_005252008.4:c.2298G>T
|
XP_005252065.1:p.Gln766His
|
|
XM_006717121.3:c.2298G>T
|
XP_006717184.1:p.Gln766His
|
|
XM_017014762.1:c.2709G>T
|
XP_016870251.1:p.Gln903His
|
|
XM_017014763.1:c.2298G>T
|
XP_016870252.1:p.Gln766His
|
|
NM_004560.4:c.2718G>T
MANE Select
|
NP_004551.2:p.Gln906His
|
|