ENST00000264499.9:c.680T>G
MANE Select
|
ENSP00000264499.4:p.Val227Gly
|
|
ENST00000264499.8:c.680T>G
|
ENSP00000264499.4:p.Val227Gly
|
|
ENST00000506636.1:c.680T>G
|
ENSP00000423626.1:p.Val227Gly
|
|
NM_018190.3:c.680T>G
|
NP_060660.2:p.Val227Gly
|
|
NM_176824.2:c.680T>G
|
NP_789794.1:p.Val227Gly
|
|
XM_005263106.2:c.683T>G
|
XP_005263163.1:p.Val228Gly
|
|
XM_011532079.1:c.728T>G
|
XP_011530381.1:p.Val243Gly
|
|
XM_011532080.1:c.725T>G
|
XP_011530382.1:p.Val242Gly
|
|
XM_011532081.1:c.728T>G
|
XP_011530383.1:p.Val243Gly
|
|
XM_005263106.4:c.683T>G
|
XP_005263163.1:p.Val228Gly
|
|
XM_011532079.3:c.728T>G
|
XP_011530381.1:p.Val243Gly
|
|
XM_011532080.3:c.725T>G
|
XP_011530382.1:p.Val242Gly
|
|
XM_011532081.3:c.728T>G
|
XP_011530383.1:p.Val243Gly
|
|
XM_017008357.2:c.680T>G
|
XP_016863846.1:p.Val227Gly
|
|
XM_017008358.2:c.683T>G
|
XP_016863847.1:p.Val228Gly
|
|
NM_176824.3:c.680T>G
MANE Select
|
NP_789794.1:p.Val227Gly
|
|
NM_018190.4:c.680T>G
|
NP_060660.2:p.Val227Gly
|
|