|
ENST00000375687.10:c.3812C>T
MANE Select
|
ENSP00000364839.4:p.Thr1271Ile
|
|
|
ENST00000646985.1:c.3629C>T
|
ENSP00000495053.1:p.Thr1210Ile
|
|
|
ENST00000647223.1:n.6165C>T
|
|
|
|
ENST00000651418.1:c.1870-1906C>T
|
ENSP00000499150.1:n.1870-1906C>T
|
|
|
ENST00000306058.9:c.3797C>T
|
ENSP00000305119.5:p.Thr1266Ile
|
|
|
ENST00000375687.8:c.3812C>T
|
ENSP00000364839.4:p.Thr1271Ile
|
|
|
ENST00000613218.4:c.3812C>T
|
ENSP00000480487.1:p.Thr1271Ile
|
|
|
ENST00000620121.4:c.3812C>T
|
ENSP00000481978.1:p.Thr1271Ile
|
|
|
NM_015338.5:c.3812C>T , LRG_630t1:c.3812C>T
|
NP_056153.2:p.Thr1271Ile
|
|
|
XM_006723727.2:c.3809C>T
|
XP_006723790.1:p.Thr1270Ile
|
|
|
XM_006723728.2:c.3782C>T
|
XP_006723791.1:p.Thr1261Ile
|
|
|
XM_006723730.2:c.3728C>T
|
XP_006723793.1:p.Thr1243Ile
|
|
|
XM_006723732.2:c.3629C>T
|
XP_006723795.1:p.Thr1210Ile
|
|
|
XM_006723733.1:c.3128C>T
|
XP_006723796.1:p.Thr1043Ile
|
|
|
XM_011528647.1:c.4076C>T
|
XP_011526949.1:p.Thr1359Ile
|
|
|
XM_011528648.1:c.4073C>T
|
XP_011526950.1:p.Thr1358Ile
|
|
|
XM_011528649.1:c.3992C>T
|
XP_011526951.1:p.Thr1331Ile
|
|
|
XM_011528650.1:c.3923C>T
|
XP_011526952.1:p.Thr1308Ile
|
|
|
XM_011528651.1:c.3791C>T
|
XP_011526953.1:p.Thr1264Ile
|
|
|
XM_011528652.1:c.3728C>T
|
XP_011526954.1:p.Thr1243Ile
|
|
|
NM_001363734.1:c.3629C>T
|
NP_001350663.1:p.Thr1210Ile
|
|
|
XM_006723727.3:c.3809C>T
|
XP_006723790.1:p.Thr1270Ile
|
|
|
XM_006723728.3:c.3782C>T
|
XP_006723791.1:p.Thr1261Ile
|
|
|
XM_006723730.4:c.3728C>T
|
XP_006723793.1:p.Thr1243Ile
|
|
|
XM_011528648.3:c.4073C>T
|
XP_011526950.1:p.Thr1358Ile
|
|
|
XM_011528652.2:c.3728C>T
|
XP_011526954.1:p.Thr1243Ile
|
|
|
XM_017027704.1:c.3728C>T
|
XP_016883193.1:p.Thr1243Ile
|
|
|
XM_017027705.1:c.3728C>T
|
XP_016883194.1:p.Thr1243Ile
|
|
|
XM_017027706.1:c.3659C>T
|
XP_016883195.1:p.Thr1220Ile
|
|
|
NM_015338.6:c.3812C>T
MANE Select
|
NP_056153.2:p.Thr1271Ile
|
|
