ENST00000375708.4:c.227G>A
MANE Select
|
ENSP00000364860.3:p.Gly76Asp
|
|
ENST00000375708.3:c.227G>A
|
ENSP00000364860.3:p.Gly76Asp
|
|
ENST00000375715.5:c.-194G>A
|
ENSP00000364867.1:n.-194G>A
|
|
ENST00000495386.5:n.490G>A
|
|
|
ENST00000546883.1:n.429G>A
|
|
|
ENST00000548585.2:n.93G>A
|
|
|
ENST00000550066.5:n.695G>A
|
|
|
NM_004560.3:c.227G>A
|
NP_004551.2:p.Gly76Asp
|
|
XM_005252008.3:c.-194G>A
|
XP_005252065.1:n.-194G>A
|
|
XM_006717121.2:c.-194G>A
|
XP_006717184.1:n.-194G>A
|
|
XM_011518721.1:c.-194G>A
|
XP_011517023.1:n.-194G>A
|
|
NM_001318204.1:c.227G>A
|
NP_001305133.1:p.Gly76Asp
|
|
XM_005252008.4:c.-194G>A
|
XP_005252065.1:n.-194G>A
|
|
XM_006717121.3:c.-194G>A
|
XP_006717184.1:n.-194G>A
|
|
XM_017014762.1:c.218G>A
|
XP_016870251.1:p.Gly73Asp
|
|
XM_017014763.1:c.-194G>A
|
XP_016870252.1:n.-194G>A
|
|
XR_001746315.1:n.470G>A
|
|
|
NM_004560.4:c.227G>A
MANE Select
|
NP_004551.2:p.Gly76Asp
|
|
NM_001318204.2:c.227G>A
|
NP_001305133.1:p.Gly76Asp
|
|