ENST00000695850.1:n.1616G>T
|
|
|
ENST00000695852.1:n.547G>T
|
|
|
ENST00000695853.1:c.*1499G>T
|
ENSP00000512218.1:n.*1499G>T
|
|
ENST00000423902.7:c.8440G>T
MANE Select
|
ENSP00000392028.1:p.Gly2814Trp
|
|
ENST00000423902.6:c.8440G>T
|
ENSP00000392028.1:p.Gly2814Trp
|
|
ENST00000524602.5:c.2293G>T
|
ENSP00000437061.1:p.Gly765Trp
|
|
ENST00000528280.1:n.486G>T
|
|
|
NM_001316690.1:c.2293G>T
|
NP_001303619.1:p.Gly765Trp
|
|
NM_017780.3:c.8440G>T
|
NP_060250.2:p.Gly2814Trp
|
|
XM_011517553.1:c.8530G>T
|
XP_011515855.1:p.Gly2844Trp
|
|
XM_011517554.1:c.8530G>T
|
XP_011515856.1:p.Gly2844Trp
|
|
XM_011517555.1:c.8527G>T
|
XP_011515857.1:p.Gly2843Trp
|
|
XM_011517556.1:c.8308G>T
|
XP_011515858.1:p.Gly2770Trp
|
|
XM_011517557.1:c.6517G>T
|
XP_011515859.1:p.Gly2173Trp
|
|
XM_011517558.1:c.6067G>T
|
XP_011515860.1:p.Gly2023Trp
|
|
XM_011517559.1:c.5275G>T
|
XP_011515861.1:p.Gly1759Trp
|
|
XM_011517553.2:c.8530G>T
|
XP_011515855.1:p.Gly2844Trp
|
|
XM_011517554.3:c.8530G>T
|
XP_011515856.1:p.Gly2844Trp
|
|
XM_011517555.2:c.8527G>T
|
XP_011515857.1:p.Gly2843Trp
|
|
XM_017013612.1:c.8530G>T
|
XP_016869101.1:p.Gly2844Trp
|
|
XM_017013613.1:c.8437G>T
|
XP_016869102.1:p.Gly2813Trp
|
|
NM_017780.4:c.8440G>T
MANE Select
|
NP_060250.2:p.Gly2814Trp
|
|