ENST00000406246.8:c.985C>T
MANE Select
|
ENSP00000384273.3:p.Arg329Ter
|
|
ENST00000308639.13:c.976C>T
|
ENSP00000311508.9:p.Arg326Ter
|
|
ENST00000406246.7:c.985C>T
|
ENSP00000384273.3:p.Arg329Ter
|
|
ENST00000525693.5:c.985C>T
|
ENSP00000432537.1:p.Arg329Ter
|
|
ENST00000526257.1:c.186C>T
|
|
|
ENST00000526283.6:c.*89C>T
|
ENSP00000435290.1:n.*89C>T
|
|
ENST00000531484.5:n.1169C>T
|
|
|
ENST00000532999.5:c.1018C>T
|
ENSP00000433526.1:p.Arg340Ter
|
|
ENST00000612991.4:c.985C>T
|
ENSP00000483705.1:p.Arg329Ter
|
|
ENST00000615805.4:c.676-32C>T
|
ENSP00000479572.1:n.676-32C>T
|
|
NM_001145138.1:c.976C>T
|
NP_001138610.1:p.Arg326Ter
|
|
NM_001243984.1:c.985C>T
|
NP_001230913.1:p.Arg329Ter
|
|
NM_001243985.1:c.985C>T
|
NP_001230914.1:p.Arg329Ter
|
|
NM_021975.3:c.985C>T
|
NP_068810.3:p.Arg329Ter
|
|
XM_011545206.1:c.772C>T
|
XP_011543508.1:p.Arg258Ter
|
|
XM_011545207.1:c.667C>T
|
XP_011543509.1:p.Arg223Ter
|
|
XM_011545206.2:c.772C>T
|
XP_011543508.1:p.Arg258Ter
|
|
XM_011545207.2:c.667C>T
|
XP_011543509.1:p.Arg223Ter
|
|
NM_021975.4:c.985C>T
MANE Select
|
NP_068810.3:p.Arg329Ter
|
|
NM_001145138.2:c.976C>T
|
NP_001138610.1:p.Arg326Ter
|
|
NM_001243984.2:c.985C>T
|
NP_001230913.1:p.Arg329Ter
|
|
NM_001243985.2:c.985C>T
|
NP_001230914.1:p.Arg329Ter
|
|