ENST00000695850.1:n.1542C>A
|
|
|
ENST00000695852.1:n.473C>A
|
|
|
ENST00000695853.1:c.*1425C>A
|
ENSP00000512218.1:n.*1425C>A
|
|
ENST00000423902.7:c.8366C>A
MANE Select
|
ENSP00000392028.1:p.Ala2789Glu
|
|
ENST00000423902.6:c.8366C>A
|
ENSP00000392028.1:p.Ala2789Glu
|
|
ENST00000524602.5:c.2219C>A
|
ENSP00000437061.1:p.Ala740Glu
|
|
ENST00000528280.1:n.412C>A
|
|
|
NM_001316690.1:c.2219C>A
|
NP_001303619.1:p.Ala740Glu
|
|
NM_017780.3:c.8366C>A
|
NP_060250.2:p.Ala2789Glu
|
|
XM_011517553.1:c.8456C>A
|
XP_011515855.1:p.Ala2819Glu
|
|
XM_011517554.1:c.8456C>A
|
XP_011515856.1:p.Ala2819Glu
|
|
XM_011517555.1:c.8453C>A
|
XP_011515857.1:p.Ala2818Glu
|
|
XM_011517556.1:c.8234C>A
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XP_011515858.1:p.Ala2745Glu
|
|
XM_011517557.1:c.6443C>A
|
XP_011515859.1:p.Ala2148Glu
|
|
XM_011517558.1:c.5993C>A
|
XP_011515860.1:p.Ala1998Glu
|
|
XM_011517559.1:c.5201C>A
|
XP_011515861.1:p.Ala1734Glu
|
|
XM_011517553.2:c.8456C>A
|
XP_011515855.1:p.Ala2819Glu
|
|
XM_011517554.3:c.8456C>A
|
XP_011515856.1:p.Ala2819Glu
|
|
XM_011517555.2:c.8453C>A
|
XP_011515857.1:p.Ala2818Glu
|
|
XM_017013612.1:c.8456C>A
|
XP_016869101.1:p.Ala2819Glu
|
|
XM_017013613.1:c.8363C>A
|
XP_016869102.1:p.Ala2788Glu
|
|
NM_017780.4:c.8366C>A
MANE Select
|
NP_060250.2:p.Ala2789Glu
|
|