ENST00000375687.10:c.3619G>T
MANE Select
|
ENSP00000364839.4:p.Val1207Phe
|
|
ENST00000646985.1:c.3436G>T
|
ENSP00000495053.1:p.Val1146Phe
|
|
ENST00000647223.1:n.5972G>T
|
|
|
ENST00000651418.1:c.1869+1750G>T
|
ENSP00000499150.1:n.1869+1750G>T
|
|
ENST00000306058.9:c.3604G>T
|
ENSP00000305119.5:p.Val1202Phe
|
|
ENST00000375687.8:c.3619G>T
|
ENSP00000364839.4:p.Val1207Phe
|
|
ENST00000613218.4:c.3619G>T
|
ENSP00000480487.1:p.Val1207Phe
|
|
ENST00000620121.4:c.3619G>T
|
ENSP00000481978.1:p.Val1207Phe
|
|
NM_015338.5:c.3619G>T , LRG_630t1:c.3619G>T
|
NP_056153.2:p.Val1207Phe
|
|
XM_006723727.2:c.3616G>T
|
XP_006723790.1:p.Val1206Phe
|
|
XM_006723728.2:c.3589G>T
|
XP_006723791.1:p.Val1197Phe
|
|
XM_006723730.2:c.3535G>T
|
XP_006723793.1:p.Val1179Phe
|
|
XM_006723732.2:c.3436G>T
|
XP_006723795.1:p.Val1146Phe
|
|
XM_006723733.1:c.2935G>T
|
XP_006723796.1:p.Val979Phe
|
|
XM_011528647.1:c.3883G>T
|
XP_011526949.1:p.Val1295Phe
|
|
XM_011528648.1:c.3880G>T
|
XP_011526950.1:p.Val1294Phe
|
|
XM_011528649.1:c.3799G>T
|
XP_011526951.1:p.Val1267Phe
|
|
XM_011528650.1:c.3730G>T
|
XP_011526952.1:p.Val1244Phe
|
|
XM_011528651.1:c.3598G>T
|
XP_011526953.1:p.Val1200Phe
|
|
XM_011528652.1:c.3535G>T
|
XP_011526954.1:p.Val1179Phe
|
|
NM_001363734.1:c.3436G>T
|
NP_001350663.1:p.Val1146Phe
|
|
XM_006723727.3:c.3616G>T
|
XP_006723790.1:p.Val1206Phe
|
|
XM_006723728.3:c.3589G>T
|
XP_006723791.1:p.Val1197Phe
|
|
XM_006723730.4:c.3535G>T
|
XP_006723793.1:p.Val1179Phe
|
|
XM_011528648.3:c.3880G>T
|
XP_011526950.1:p.Val1294Phe
|
|
XM_011528652.2:c.3535G>T
|
XP_011526954.1:p.Val1179Phe
|
|
XM_017027704.1:c.3535G>T
|
XP_016883193.1:p.Val1179Phe
|
|
XM_017027705.1:c.3535G>T
|
XP_016883194.1:p.Val1179Phe
|
|
XM_017027706.1:c.3466G>T
|
XP_016883195.1:p.Val1156Phe
|
|
NM_015338.6:c.3619G>T
MANE Select
|
NP_056153.2:p.Val1207Phe
|
|