ENST00000274376.11:c.406C>T
MANE Select
|
ENSP00000274376.6:p.Pro136Ser
|
|
ENST00000274376.10:c.406C>T
|
ENSP00000274376.6:p.Pro136Ser
|
|
ENST00000515800.6:c.406C>T
|
ENSP00000423395.2:p.Pro136Ser
|
|
NM_002890.2:c.406C>T
|
NP_002881.1:p.Pro136Ser
|
|
XM_011543525.1:c.406C>T
|
XP_011541827.1:p.Pro136Ser
|
|
XM_011543526.1:c.406C>T
|
XP_011541828.1:p.Pro136Ser
|
|
XM_011543527.1:c.406C>T
|
XP_011541829.1:p.Pro136Ser
|
|
XM_011543525.2:c.406C>T
|
XP_011541827.1:p.Pro136Ser
|
|
XM_011543527.3:c.406C>T
|
XP_011541829.1:p.Pro136Ser
|
|
NM_002890.3:c.406C>T
MANE Select
|
NP_002881.1:p.Pro136Ser
|
|