ENST00000426263.10:c.797C>T
MANE Select
|
ENSP00000416293.2:p.Pro266Leu
|
|
ENST00000669445.1:c.127C>T
|
|
|
ENST00000674765.1:c.797C>T
|
ENSP00000501811.1:p.Pro266Leu
|
|
ENST00000675112.1:n.820C>T
|
|
|
ENST00000676254.1:n.1246C>T
|
|
|
ENST00000426263.7:c.797C>T
|
ENSP00000416293.2:p.Pro266Leu
|
|
ENST00000439722.2:c.676C>T
|
ENSP00000395521.2:n.676C>T
|
|
ENST00000475162.3:c.415+963C>T
|
|
|
ENST00000630287.2:c.*112C>T
|
ENSP00000486694.1:n.*112C>T
|
|
NM_006516.2:c.797C>T
|
NP_006507.2:p.Pro266Leu
|
|
NM_006516.3:c.797C>T
|
NP_006507.2:p.Pro266Leu
|
|
NM_006516.4:c.797C>T
MANE Select
|
NP_006507.2:p.Pro266Leu
|
|