|
NM_001851.6:c.352C>T
MANE Select
|
NP_001842.3:p.Arg118Ter
|
|
ENST00000357250.11:c.352C>T
MANE Select
|
ENSP00000349790.6:p.Arg118Ter
|
|
NM_001377291.1:c.352C>T
|
NP_001364220.1:p.Arg118Ter
|
|
NM_001851.4:c.352C>T
|
NP_001842.3:p.Arg118Ter
|
|
NM_001851.5:c.352C>T
|
NP_001842.3:p.Arg118Ter
|
|
ENST00000357250.10:c.352C>T
|
ENSP00000349790.6:p.Arg118Ter
|
|
ENST00000370496.3:c.352C>T
|
ENSP00000359527.3:p.Arg118Ter
|
|
XM_011535429.1:c.352C>T
|
XP_011533731.1:p.Arg118Ter
|
|
XM_011535429.3:c.352C>T
|
XP_011533731.1:p.Arg118Ter
|
|
XM_017010246.2:c.-12-186C>T
|
XP_016865735.1:n.-12-186C>T
|