ENST00000375708.4:c.2066G>A
MANE Select
|
ENSP00000364860.3:p.Gly689Asp
|
|
ENST00000375708.3:c.2066G>A
|
ENSP00000364860.3:p.Gly689Asp
|
|
ENST00000375715.5:c.1646G>A
|
ENSP00000364867.1:p.Gly549Asp
|
|
ENST00000550066.5:n.2534G>A
|
|
|
NM_004560.3:c.2066G>A
|
NP_004551.2:p.Gly689Asp
|
|
XM_005252008.3:c.1646G>A
|
XP_005252065.1:p.Gly549Asp
|
|
XM_005252009.3:c.863G>A
|
XP_005252066.1:p.Gly288Asp
|
|
XM_006717121.2:c.1646G>A
|
XP_006717184.1:p.Gly549Asp
|
|
XM_011518721.1:c.1646G>A
|
XP_011517023.1:p.Gly549Asp
|
|
XM_005252008.4:c.1646G>A
|
XP_005252065.1:p.Gly549Asp
|
|
XM_006717121.3:c.1646G>A
|
XP_006717184.1:p.Gly549Asp
|
|
XM_017014762.1:c.2057G>A
|
XP_016870251.1:p.Gly686Asp
|
|
XM_017014763.1:c.1646G>A
|
XP_016870252.1:p.Gly549Asp
|
|
NM_004560.4:c.2066G>A
MANE Select
|
NP_004551.2:p.Gly689Asp
|
|