ENST00000295754.10:c.937C>T
MANE Select
|
ENSP00000295754.5:p.Arg313Trp
|
|
ENST00000672866.1:n.2533C>T
|
|
|
ENST00000295754.9:c.937C>T
|
ENSP00000295754.5:p.Arg313Trp
|
|
ENST00000359013.4:c.1012C>T
|
ENSP00000351905.4:p.Arg338Trp
|
|
NM_001024847.2:c.1012C>T , LRG_779t1:c.1012C>T
|
NP_001020018.1:p.Arg338Trp
|
|
NM_003242.5:c.937C>T
|
NP_003233.4:p.Arg313Trp
|
|
XM_011534043.1:c.964C>T
|
XP_011532345.1:p.Arg322Trp
|
|
XM_011534044.1:c.889C>T
|
XP_011532346.1:p.Arg297Trp
|
|
XM_011534045.1:c.832C>T
|
XP_011532347.1:p.Arg278Trp
|
|
XM_011534043.2:c.964C>T
|
XP_011532345.1:p.Arg322Trp
|
|
XM_011534045.3:c.832C>T
|
XP_011532347.1:p.Arg278Trp
|
|
XM_017007106.1:c.832C>T
|
XP_016862595.1:p.Arg278Trp
|
|
NM_003242.6:c.937C>T
MANE Select
|
NP_003233.4:p.Arg313Trp
|
|