ENST00000347132.10:c.1293-297T>C
MANE Select
|
ENSP00000262916.6:n.1293-297T>C
|
|
ENST00000347132.9:c.1293-297T>C
|
ENSP00000262916.6:n.1293-297T>C
|
|
ENST00000443478.3:c.874-297T>C
|
|
|
ENST00000506017.1:n.612-297T>C
|
|
|
ENST00000509682.6:c.1131-297T>C
|
ENSP00000423756.2:n.1131-297T>C
|
|
NM_004700.3:c.1293-297T>C
|
NP_004691.2:n.1293-297T>C
|
|
NM_172163.2:c.1131-297T>C
|
NP_751895.1:n.1131-297T>C
|
|
XM_011542418.1:c.1305T>C
|
XP_011540720.1:p.Asp435=
|
|
XR_946798.1:n.1299-297T>C
|
|
|
XR_946799.1:n.1299-297T>C
|
|
|
XR_946800.1:n.1048-297T>C
|
|
|
XM_017002792.1:c.276-297T>C
|
XP_016858281.1:n.276-297T>C
|
|
NM_004700.4:c.1293-297T>C
MANE Select
|
NP_004691.2:n.1293-297T>C
|
|
NM_172163.3:c.1131-297T>C
|
NP_751895.1:n.1131-297T>C
|
|