ENST00000695850.1:n.808T>G
|
|
|
ENST00000695851.1:n.12T>G
|
|
|
ENST00000695853.1:c.*691T>G
|
ENSP00000512218.1:n.*691T>G
|
|
ENST00000423902.7:c.7632T>G
MANE Select
|
ENSP00000392028.1:p.Ala2544=
|
|
ENST00000423902.6:c.7632T>G
|
ENSP00000392028.1:p.Ala2544=
|
|
ENST00000524602.5:c.1717-1302T>G
|
ENSP00000437061.1:n.1717-1302T>G
|
|
ENST00000531695.1:n.56T>G
|
|
|
ENST00000618450.1:n.24T>G
|
|
|
NM_001316690.1:c.1717-1302T>G
|
NP_001303619.1:n.1717-1302T>G
|
|
NM_017780.3:c.7632T>G
|
NP_060250.2:p.Ala2544=
|
|
XM_011517553.1:c.7722T>G
|
XP_011515855.1:p.Ala2574=
|
|
XM_011517554.1:c.7722T>G
|
XP_011515856.1:p.Ala2574=
|
|
XM_011517555.1:c.7719T>G
|
XP_011515857.1:p.Ala2573=
|
|
XM_011517556.1:c.7699-1269T>G
|
XP_011515858.1:n.7699-1269T>G
|
|
XM_011517557.1:c.5709T>G
|
XP_011515859.1:p.Ala1903=
|
|
XM_011517558.1:c.5259T>G
|
XP_011515860.1:p.Ala1753=
|
|
XM_011517559.1:c.4467T>G
|
XP_011515861.1:p.Ala1489=
|
|
XM_011517553.2:c.7722T>G
|
XP_011515855.1:p.Ala2574=
|
|
XM_011517554.3:c.7722T>G
|
XP_011515856.1:p.Ala2574=
|
|
XM_011517555.2:c.7719T>G
|
XP_011515857.1:p.Ala2573=
|
|
XM_017013612.1:c.7722T>G
|
XP_016869101.1:p.Ala2574=
|
|
XM_017013613.1:c.7629T>G
|
XP_016869102.1:p.Ala2543=
|
|
NM_017780.4:c.7632T>G
MANE Select
|
NP_060250.2:p.Ala2544=
|
|