ENST00000695850.1:n.1317C>T
|
|
|
ENST00000695852.1:n.248C>T
|
|
|
ENST00000695853.1:c.*1200C>T
|
ENSP00000512218.1:n.*1200C>T
|
|
ENST00000423902.7:c.8141C>T
MANE Select
|
ENSP00000392028.1:p.Ala2714Val
|
|
ENST00000423902.6:c.8141C>T
|
ENSP00000392028.1:p.Ala2714Val
|
|
ENST00000524602.5:c.1994C>T
|
ENSP00000437061.1:p.Ala665Val
|
|
ENST00000528280.1:n.187C>T
|
|
|
ENST00000532149.1:n.563C>T
|
|
|
ENST00000618450.1:n.4177C>T
|
|
|
NM_001316690.1:c.1994C>T
|
NP_001303619.1:p.Ala665Val
|
|
NM_017780.3:c.8141C>T
|
NP_060250.2:p.Ala2714Val
|
|
XM_011517553.1:c.8231C>T
|
XP_011515855.1:p.Ala2744Val
|
|
XM_011517554.1:c.8231C>T
|
XP_011515856.1:p.Ala2744Val
|
|
XM_011517555.1:c.8228C>T
|
XP_011515857.1:p.Ala2743Val
|
|
XM_011517556.1:c.8009C>T
|
XP_011515858.1:p.Ala2670Val
|
|
XM_011517557.1:c.6218C>T
|
XP_011515859.1:p.Ala2073Val
|
|
XM_011517558.1:c.5768C>T
|
XP_011515860.1:p.Ala1923Val
|
|
XM_011517559.1:c.4976C>T
|
XP_011515861.1:p.Ala1659Val
|
|
XM_011517553.2:c.8231C>T
|
XP_011515855.1:p.Ala2744Val
|
|
XM_011517554.3:c.8231C>T
|
XP_011515856.1:p.Ala2744Val
|
|
XM_011517555.2:c.8228C>T
|
XP_011515857.1:p.Ala2743Val
|
|
XM_017013612.1:c.8231C>T
|
XP_016869101.1:p.Ala2744Val
|
|
XM_017013613.1:c.8138C>T
|
XP_016869102.1:p.Ala2713Val
|
|
NM_017780.4:c.8141C>T
MANE Select
|
NP_060250.2:p.Ala2714Val
|
|