ENST00000578493.2:n.888A=
|
|
|
ENST00000699291.1:c.680A=
|
ENSP00000514272.1:n.680A=
|
|
ENST00000699292.1:n.595A=
|
|
|
ENST00000225275.4:c.1555A=
MANE Select
|
ENSP00000225275.3:p.Met519=
|
|
ENST00000225275.3:c.1555A=
|
ENSP00000225275.3:p.Met519=
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|
ENST00000577220.1:c.13A=
|
ENSP00000464668.1:p.Met5=
|
|
NM_000250.1:c.1555A= , LRG_84t1:c.1555A=
|
NP_000241.1:p.Met519=
|
|
XM_011524821.1:c.1741A=
|
XP_011523123.1:p.Met581=
|
|
XM_011524822.1:c.1270A=
|
XP_011523124.1:p.Met424=
|
|
XM_011524823.1:c.*104A=
|
XP_011523125.1:n.*104A=
|
|
NM_000250.2:c.1555A=
MANE Select
|
NP_000241.1:p.Met519=
|
|