ENST00000695850.1:n.976T>G
|
|
|
ENST00000695851.1:n.180T>G
|
|
|
ENST00000695853.1:c.*859T>G
|
ENSP00000512218.1:n.*859T>G
|
|
ENST00000423902.7:c.7800T>G
MANE Select
|
ENSP00000392028.1:p.Thr2600=
|
|
ENST00000423902.6:c.7800T>G
|
ENSP00000392028.1:p.Thr2600=
|
|
ENST00000524602.5:c.1717-1134T>G
|
ENSP00000437061.1:n.1717-1134T>G
|
|
ENST00000531695.1:n.224T>G
|
|
|
ENST00000618450.1:n.192T>G
|
|
|
NM_001316690.1:c.1717-1134T>G
|
NP_001303619.1:n.1717-1134T>G
|
|
NM_017780.3:c.7800T>G
|
NP_060250.2:p.Thr2600=
|
|
XM_011517553.1:c.7890T>G
|
XP_011515855.1:p.Thr2630=
|
|
XM_011517554.1:c.7890T>G
|
XP_011515856.1:p.Thr2630=
|
|
XM_011517555.1:c.7887T>G
|
XP_011515857.1:p.Thr2629=
|
|
XM_011517556.1:c.7699-1101T>G
|
XP_011515858.1:n.7699-1101T>G
|
|
XM_011517557.1:c.5877T>G
|
XP_011515859.1:p.Thr1959=
|
|
XM_011517558.1:c.5427T>G
|
XP_011515860.1:p.Thr1809=
|
|
XM_011517559.1:c.4635T>G
|
XP_011515861.1:p.Thr1545=
|
|
XM_011517553.2:c.7890T>G
|
XP_011515855.1:p.Thr2630=
|
|
XM_011517554.3:c.7890T>G
|
XP_011515856.1:p.Thr2630=
|
|
XM_011517555.2:c.7887T>G
|
XP_011515857.1:p.Thr2629=
|
|
XM_017013612.1:c.7890T>G
|
XP_016869101.1:p.Thr2630=
|
|
XM_017013613.1:c.7797T>G
|
XP_016869102.1:p.Thr2599=
|
|
NM_017780.4:c.7800T>G
MANE Select
|
NP_060250.2:p.Thr2600=
|
|