ENST00000261978.9:c.5351C>G
MANE Select
|
ENSP00000261978.4:p.Pro1784Arg
|
|
ENST00000261978.8:c.5351C>G
|
ENSP00000261978.4:p.Pro1784Arg
|
|
ENST00000553939.5:c.*130C>G
|
ENSP00000452110.1:n.*130C>G
|
|
ENST00000554861.1:n.569C>G
|
|
|
ENST00000556690.5:c.5219C>G
|
ENSP00000451477.1:p.Pro1740Arg
|
|
NM_000428.2:c.5351C>G
|
NP_000419.1:p.Pro1784Arg
|
|
XM_011536765.1:c.4970C>G
|
XP_011535067.1:p.Pro1657Arg
|
|
XM_011536766.1:c.4892C>G
|
XP_011535068.1:p.Pro1631Arg
|
|
XM_011536767.1:c.4868C>G
|
XP_011535069.1:p.Pro1623Arg
|
|
XM_011536765.2:c.4970C>G
|
XP_011535067.1:p.Pro1657Arg
|
|
NM_000428.3:c.5351C>G
MANE Select
|
NP_000419.1:p.Pro1784Arg
|
|