ENST00000695850.1:n.1329G>T
|
|
|
ENST00000695852.1:n.260G>T
|
|
|
ENST00000695853.1:c.*1212G>T
|
ENSP00000512218.1:n.*1212G>T
|
|
ENST00000423902.7:c.8153G>T
MANE Select
|
ENSP00000392028.1:p.Gly2718Val
|
|
ENST00000423902.6:c.8153G>T
|
ENSP00000392028.1:p.Gly2718Val
|
|
ENST00000524602.5:c.2006G>T
|
ENSP00000437061.1:p.Gly669Val
|
|
ENST00000528280.1:n.199G>T
|
|
|
ENST00000532149.1:n.575G>T
|
|
|
ENST00000618450.1:n.4189G>T
|
|
|
NM_001316690.1:c.2006G>T
|
NP_001303619.1:p.Gly669Val
|
|
NM_017780.3:c.8153G>T
|
NP_060250.2:p.Gly2718Val
|
|
XM_011517553.1:c.8243G>T
|
XP_011515855.1:p.Gly2748Val
|
|
XM_011517554.1:c.8243G>T
|
XP_011515856.1:p.Gly2748Val
|
|
XM_011517555.1:c.8240G>T
|
XP_011515857.1:p.Gly2747Val
|
|
XM_011517556.1:c.8021G>T
|
XP_011515858.1:p.Gly2674Val
|
|
XM_011517557.1:c.6230G>T
|
XP_011515859.1:p.Gly2077Val
|
|
XM_011517558.1:c.5780G>T
|
XP_011515860.1:p.Gly1927Val
|
|
XM_011517559.1:c.4988G>T
|
XP_011515861.1:p.Gly1663Val
|
|
XM_011517553.2:c.8243G>T
|
XP_011515855.1:p.Gly2748Val
|
|
XM_011517554.3:c.8243G>T
|
XP_011515856.1:p.Gly2748Val
|
|
XM_011517555.2:c.8240G>T
|
XP_011515857.1:p.Gly2747Val
|
|
XM_017013612.1:c.8243G>T
|
XP_016869101.1:p.Gly2748Val
|
|
XM_017013613.1:c.8150G>T
|
XP_016869102.1:p.Gly2717Val
|
|
NM_017780.4:c.8153G>T
MANE Select
|
NP_060250.2:p.Gly2718Val
|
|