|
NM_003036.4:c.1274C>T
MANE Select
|
NP_003027.1:p.Ala425Val
|
|
ENST00000378536.5:c.1274C>T
MANE Select
|
ENSP00000367797.4:p.Ala425Val
|
|
NM_003036.3:c.1274C>T
|
NP_003027.1:p.Ala425Val
|
|
ENST00000378536.4:c.1274C>T
|
ENSP00000367797.4:p.Ala425Val
|
|
ENST00000507179.1:n.257C>T
|
|
|
ENST00000704337.1:n.442C>T
|
|
|
XM_005244775.2:c.1274C>T
|
XP_005244832.1:p.Ala425Val
|
|
XM_005244775.3:c.1274C>T
|
XP_005244832.1:p.Ala425Val
|
|
XM_005244776.3:c.404C>T
|
XP_005244833.1:p.Ala135Val
|
|
XM_005244776.4:c.404C>T
|
XP_005244833.1:p.Ala135Val
|
|
XM_017002128.1:c.782C>T
|
XP_016857617.1:p.Ala261Val
|