ENST00000303941.4:c.1325G>A
MANE Select
|
ENSP00000306678.3:p.Gly442Asp
|
|
ENST00000303941.3:c.1325G>A
|
ENSP00000306678.3:p.Gly442Asp
|
|
NM_178510.1:c.1325G>A
|
NP_848605.1:p.Gly442Asp
|
|
XM_011542736.1:c.1358G>A
|
XP_011541038.1:p.Gly453Asp
|
|
XM_011542737.1:c.1328G>A
|
XP_011541039.1:p.Gly443Asp
|
|
XM_011542738.1:c.1136G>A
|
XP_011541040.1:p.Gly379Asp
|
|
XM_011542736.2:c.1358G>A
|
XP_011541038.1:p.Gly453Asp
|
|
XM_011542737.2:c.1328G>A
|
XP_011541039.1:p.Gly443Asp
|
|
XM_011542738.2:c.1136G>A
|
XP_011541040.1:p.Gly379Asp
|
|
XM_017017475.1:c.1355G>A
|
XP_016872964.1:p.Gly452Asp
|
|
NM_178510.2:c.1325G>A
MANE Select
|
NP_848605.1:p.Gly442Asp
|
|