ENST00000346342.8:c.1133G>T
MANE Select
|
ENSP00000329546.4:p.Cys378Phe
|
|
ENST00000346342.7:c.1133G>T
|
ENSP00000329546.3:p.Cys378Phe
|
|
ENST00000375581.3:c.1199G>T
|
ENSP00000364731.3:p.Cys400Phe
|
|
ENST00000541084.5:c.947G>T
|
ENSP00000442051.2:p.Cys316Phe
|
|
NM_000131.4:c.1199G>T , LRG_554t1:c.1199G>T
|
NP_000122.1:p.Cys400Phe
|
|
NM_001267554.1:c.947G>T
|
NP_001254483.1:p.Cys316Phe
|
|
NM_019616.3:c.1133G>T , LRG_554t2:c.1133G>T
|
NP_062562.1:p.Cys378Phe
|
|
NR_051961.1:n.1220G>T
|
|
|
XM_006719963.2:c.992G>T
|
XP_006720026.1:p.Cys331Phe
|
|
XM_011537474.1:c.1241G>T
|
XP_011535776.1:p.Cys414Phe
|
|
XM_011537475.1:c.1055G>T
|
XP_011535777.1:p.Cys352Phe
|
|
XM_011537476.1:c.893G>T
|
XP_011535778.1:p.Cys298Phe
|
|
XM_011537477.1:c.1202G>T
|
XP_011535779.1:p.Cys401Phe
|
|
XM_006719963.3:c.1037G>T
|
XP_006720026.2:p.Cys346Phe
|
|
XM_011537474.2:c.1286G>T
|
XP_011535776.2:p.Cys429Phe
|
|
XM_011537475.2:c.1100G>T
|
XP_011535777.2:p.Cys367Phe
|
|
XM_011537476.2:c.893G>T
|
XP_011535778.1:p.Cys298Phe
|
|
NM_019616.4:c.1133G>T
MANE Select
|
NP_062562.1:p.Cys378Phe
|
|
NR_051961.2:n.1217G>T
|
|
|
NM_001267554.2:c.947G>T
|
NP_001254483.1:p.Cys316Phe
|
|