ENST00000695850.1:n.1495G>T
|
|
|
ENST00000695852.1:n.426G>T
|
|
|
ENST00000695853.1:c.*1378G>T
|
ENSP00000512218.1:n.*1378G>T
|
|
ENST00000423902.7:c.8319G>T
MANE Select
|
ENSP00000392028.1:p.Met2773Ile
|
|
ENST00000423902.6:c.8319G>T
|
ENSP00000392028.1:p.Met2773Ile
|
|
ENST00000524602.5:c.2172G>T
|
ENSP00000437061.1:p.Met724Ile
|
|
ENST00000528280.1:n.365G>T
|
|
|
NM_001316690.1:c.2172G>T
|
NP_001303619.1:p.Met724Ile
|
|
NM_017780.3:c.8319G>T
|
NP_060250.2:p.Met2773Ile
|
|
XM_011517553.1:c.8409G>T
|
XP_011515855.1:p.Met2803Ile
|
|
XM_011517554.1:c.8409G>T
|
XP_011515856.1:p.Met2803Ile
|
|
XM_011517555.1:c.8406G>T
|
XP_011515857.1:p.Met2802Ile
|
|
XM_011517556.1:c.8187G>T
|
XP_011515858.1:p.Met2729Ile
|
|
XM_011517557.1:c.6396G>T
|
XP_011515859.1:p.Met2132Ile
|
|
XM_011517558.1:c.5946G>T
|
XP_011515860.1:p.Met1982Ile
|
|
XM_011517559.1:c.5154G>T
|
XP_011515861.1:p.Met1718Ile
|
|
XM_011517553.2:c.8409G>T
|
XP_011515855.1:p.Met2803Ile
|
|
XM_011517554.3:c.8409G>T
|
XP_011515856.1:p.Met2803Ile
|
|
XM_011517555.2:c.8406G>T
|
XP_011515857.1:p.Met2802Ile
|
|
XM_017013612.1:c.8409G>T
|
XP_016869101.1:p.Met2803Ile
|
|
XM_017013613.1:c.8316G>T
|
XP_016869102.1:p.Met2772Ile
|
|
NM_017780.4:c.8319G>T
MANE Select
|
NP_060250.2:p.Met2773Ile
|
|