ENST00000375687.10:c.3563T>A
MANE Select
|
ENSP00000364839.4:p.Leu1188His
|
|
ENST00000646985.1:c.3380T>A
|
ENSP00000495053.1:p.Leu1127His
|
|
ENST00000647223.1:n.5916T>A
|
|
|
ENST00000651418.1:c.1869+1694T>A
|
ENSP00000499150.1:n.1869+1694T>A
|
|
ENST00000306058.9:c.3548T>A
|
ENSP00000305119.5:p.Leu1183His
|
|
ENST00000375687.8:c.3563T>A
|
ENSP00000364839.4:p.Leu1188His
|
|
ENST00000613218.4:c.3563T>A
|
ENSP00000480487.1:p.Leu1188His
|
|
ENST00000620121.4:c.3563T>A
|
ENSP00000481978.1:p.Leu1188His
|
|
NM_015338.5:c.3563T>A , LRG_630t1:c.3563T>A
|
NP_056153.2:p.Leu1188His
|
|
XM_006723727.2:c.3560T>A
|
XP_006723790.1:p.Leu1187His
|
|
XM_006723728.2:c.3533T>A
|
XP_006723791.1:p.Leu1178His
|
|
XM_006723730.2:c.3479T>A
|
XP_006723793.1:p.Leu1160His
|
|
XM_006723732.2:c.3380T>A
|
XP_006723795.1:p.Leu1127His
|
|
XM_006723733.1:c.2879T>A
|
XP_006723796.1:p.Leu960His
|
|
XM_011528647.1:c.3827T>A
|
XP_011526949.1:p.Leu1276His
|
|
XM_011528648.1:c.3824T>A
|
XP_011526950.1:p.Leu1275His
|
|
XM_011528649.1:c.3743T>A
|
XP_011526951.1:p.Leu1248His
|
|
XM_011528650.1:c.3674T>A
|
XP_011526952.1:p.Leu1225His
|
|
XM_011528651.1:c.3542T>A
|
XP_011526953.1:p.Leu1181His
|
|
XM_011528652.1:c.3479T>A
|
XP_011526954.1:p.Leu1160His
|
|
NM_001363734.1:c.3380T>A
|
NP_001350663.1:p.Leu1127His
|
|
XM_006723727.3:c.3560T>A
|
XP_006723790.1:p.Leu1187His
|
|
XM_006723728.3:c.3533T>A
|
XP_006723791.1:p.Leu1178His
|
|
XM_006723730.4:c.3479T>A
|
XP_006723793.1:p.Leu1160His
|
|
XM_011528648.3:c.3824T>A
|
XP_011526950.1:p.Leu1275His
|
|
XM_011528652.2:c.3479T>A
|
XP_011526954.1:p.Leu1160His
|
|
XM_017027704.1:c.3479T>A
|
XP_016883193.1:p.Leu1160His
|
|
XM_017027705.1:c.3479T>A
|
XP_016883194.1:p.Leu1160His
|
|
XM_017027706.1:c.3410T>A
|
XP_016883195.1:p.Leu1137His
|
|
NM_015338.6:c.3563T>A
MANE Select
|
NP_056153.2:p.Leu1188His
|
|