ENST00000295754.10:c.1300A=
MANE Select
|
ENSP00000295754.5:p.Met434=
|
|
ENST00000672866.1:n.2896A=
|
|
|
ENST00000673203.1:n.178A=
|
|
|
ENST00000295754.9:c.1300A=
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ENSP00000295754.5:p.Met434=
|
|
ENST00000359013.4:c.1375A=
|
ENSP00000351905.4:p.Met459=
|
|
NM_001024847.2:c.1375A= , LRG_779t1:c.1375A=
|
NP_001020018.1:p.Met459=
|
|
NM_003242.5:c.1300A=
|
NP_003233.4:p.Met434=
|
|
XM_011534043.1:c.1327A=
|
XP_011532345.1:p.Met443=
|
|
XM_011534044.1:c.1252A=
|
XP_011532346.1:p.Met418=
|
|
XM_011534045.1:c.1195A=
|
XP_011532347.1:p.Met399=
|
|
XM_011534043.2:c.1327A=
|
XP_011532345.1:p.Met443=
|
|
XM_011534045.3:c.1195A=
|
XP_011532347.1:p.Met399=
|
|
XM_017007106.1:c.1195A=
|
XP_016862595.1:p.Met399=
|
|
NM_003242.6:c.1300A=
MANE Select
|
NP_003233.4:p.Met434=
|
|