ENST00000695850.1:n.1557C>A
|
|
|
ENST00000695852.1:n.488C>A
|
|
|
ENST00000695853.1:c.*1440C>A
|
ENSP00000512218.1:n.*1440C>A
|
|
ENST00000423902.7:c.8381C>A
MANE Select
|
ENSP00000392028.1:p.Ala2794Asp
|
|
ENST00000423902.6:c.8381C>A
|
ENSP00000392028.1:p.Ala2794Asp
|
|
ENST00000524602.5:c.2234C>A
|
ENSP00000437061.1:p.Ala745Asp
|
|
ENST00000528280.1:n.427C>A
|
|
|
NM_001316690.1:c.2234C>A
|
NP_001303619.1:p.Ala745Asp
|
|
NM_017780.3:c.8381C>A
|
NP_060250.2:p.Ala2794Asp
|
|
XM_011517553.1:c.8471C>A
|
XP_011515855.1:p.Ala2824Asp
|
|
XM_011517554.1:c.8471C>A
|
XP_011515856.1:p.Ala2824Asp
|
|
XM_011517555.1:c.8468C>A
|
XP_011515857.1:p.Ala2823Asp
|
|
XM_011517556.1:c.8249C>A
|
XP_011515858.1:p.Ala2750Asp
|
|
XM_011517557.1:c.6458C>A
|
XP_011515859.1:p.Ala2153Asp
|
|
XM_011517558.1:c.6008C>A
|
XP_011515860.1:p.Ala2003Asp
|
|
XM_011517559.1:c.5216C>A
|
XP_011515861.1:p.Ala1739Asp
|
|
XM_011517553.2:c.8471C>A
|
XP_011515855.1:p.Ala2824Asp
|
|
XM_011517554.3:c.8471C>A
|
XP_011515856.1:p.Ala2824Asp
|
|
XM_011517555.2:c.8468C>A
|
XP_011515857.1:p.Ala2823Asp
|
|
XM_017013612.1:c.8471C>A
|
XP_016869101.1:p.Ala2824Asp
|
|
XM_017013613.1:c.8378C>A
|
XP_016869102.1:p.Ala2793Asp
|
|
NM_017780.4:c.8381C>A
MANE Select
|
NP_060250.2:p.Ala2794Asp
|
|