ENST00000356839.10:c.1390A>G
MANE Select
|
ENSP00000349297.5:p.Thr464Ala
|
|
ENST00000322910.9:c.*1345A>G
|
ENSP00000325395.5:n.*1345A>G
|
|
ENST00000350303.9:c.1324A>G
|
ENSP00000344152.5:p.Thr442Ala
|
|
ENST00000356839.9:c.1390A>G
|
ENSP00000349297.5:p.Thr464Ala
|
|
ENST00000542255.6:c.248A>G
|
|
|
ENST00000543245.6:c.1459A>G
|
ENSP00000438689.2:p.Thr487Ala
|
|
ENST00000578711.1:n.521A>G
|
|
|
ENST00000579425.5:n.506A>G
|
|
|
ENST00000579546.1:c.227A>G
|
|
|
ENST00000579894.5:n.101A>G
|
|
|
ENST00000583074.5:n.109A>G
|
|
|
ENST00000583850.5:n.165A>G
|
|
|
ENST00000583858.5:c.419A>G
|
|
|
ENST00000585203.6:n.581A>G
|
|
|
NM_000018.3:c.1390A>G
|
NP_000009.1:p.Thr464Ala
|
|
NM_001033859.2:c.1324A>G
|
NP_001029031.1:p.Thr442Ala
|
|
NM_001270447.1:c.1459A>G
|
NP_001257376.1:p.Thr487Ala
|
|
NM_001270448.1:c.1162A>G
|
NP_001257377.1:p.Thr388Ala
|
|
XM_006721516.2:c.1390A>G
|
XP_006721579.2:p.Thr464Ala
|
|
XM_011523829.1:c.1390A>G
|
XP_011522131.1:p.Thr464Ala
|
|
XM_011523830.1:c.1390A>G
|
XP_011522132.1:p.Thr464Ala
|
|
XR_934021.1:n.1497A>G
|
|
|
XR_934022.1:n.1497A>G
|
|
|
XR_934023.1:n.1497A>G
|
|
|
XM_006721516.3:c.1390A>G
|
XP_006721579.2:p.Thr464Ala
|
|
XM_011523829.2:c.1390A>G
|
XP_011522131.1:p.Thr464Ala
|
|
XM_011523830.2:c.1390A>G
|
XP_011522132.1:p.Thr464Ala
|
|
XM_024450741.1:c.1390A>G
|
XP_024306509.1:p.Thr464Ala
|
|
XR_934021.2:n.1449A>G
|
|
|
XR_934022.2:n.1449A>G
|
|
|
XR_934023.2:n.1449A>G
|
|
|
NM_000018.4:c.1390A>G
MANE Select
|
NP_000009.1:p.Thr464Ala
|
|
NM_001033859.3:c.1324A>G
|
NP_001029031.1:p.Thr442Ala
|
|
NM_001270447.2:c.1459A>G
|
NP_001257376.1:p.Thr487Ala
|
|
NM_001270448.2:c.1162A>G
|
NP_001257377.1:p.Thr388Ala
|
|