ENST00000695850.1:n.1368C>T
|
|
|
ENST00000695852.1:n.299C>T
|
|
|
ENST00000695853.1:c.*1251C>T
|
ENSP00000512218.1:n.*1251C>T
|
|
ENST00000423902.7:c.8192C>T
MANE Select
|
ENSP00000392028.1:p.Ala2731Val
|
|
ENST00000423902.6:c.8192C>T
|
ENSP00000392028.1:p.Ala2731Val
|
|
ENST00000524602.5:c.2045C>T
|
ENSP00000437061.1:p.Ala682Val
|
|
ENST00000528280.1:n.238C>T
|
|
|
ENST00000532149.1:n.614C>T
|
|
|
NM_001316690.1:c.2045C>T
|
NP_001303619.1:p.Ala682Val
|
|
NM_017780.3:c.8192C>T
|
NP_060250.2:p.Ala2731Val
|
|
XM_011517553.1:c.8282C>T
|
XP_011515855.1:p.Ala2761Val
|
|
XM_011517554.1:c.8282C>T
|
XP_011515856.1:p.Ala2761Val
|
|
XM_011517555.1:c.8279C>T
|
XP_011515857.1:p.Ala2760Val
|
|
XM_011517556.1:c.8060C>T
|
XP_011515858.1:p.Ala2687Val
|
|
XM_011517557.1:c.6269C>T
|
XP_011515859.1:p.Ala2090Val
|
|
XM_011517558.1:c.5819C>T
|
XP_011515860.1:p.Ala1940Val
|
|
XM_011517559.1:c.5027C>T
|
XP_011515861.1:p.Ala1676Val
|
|
XM_011517553.2:c.8282C>T
|
XP_011515855.1:p.Ala2761Val
|
|
XM_011517554.3:c.8282C>T
|
XP_011515856.1:p.Ala2761Val
|
|
XM_011517555.2:c.8279C>T
|
XP_011515857.1:p.Ala2760Val
|
|
XM_017013612.1:c.8282C>T
|
XP_016869101.1:p.Ala2761Val
|
|
XM_017013613.1:c.8189C>T
|
XP_016869102.1:p.Ala2730Val
|
|
NM_017780.4:c.8192C>T
MANE Select
|
NP_060250.2:p.Ala2731Val
|
|