ENST00000295897.9:c.56G>T
MANE Select
|
ENSP00000295897.4:p.Arg19Met
|
|
ENST00000295897.8:c.56G>T
|
ENSP00000295897.4:p.Arg19Met
|
|
ENST00000401494.7:c.56G>T
|
ENSP00000384695.3:p.Arg19Met
|
|
ENST00000415165.6:c.56G>T
|
ENSP00000401820.2:p.Arg19Met
|
|
ENST00000441319.5:c.62G>T
|
ENSP00000392541.1:p.Arg21Met
|
|
ENST00000476441.6:c.56G>T
|
ENSP00000423727.1:p.Arg19Met
|
|
ENST00000503124.5:c.-125G>T
|
ENSP00000421027.1:n.-125G>T
|
|
ENST00000509063.5:c.56G>T
|
ENSP00000422784.1:p.Arg19Met
|
|
ENST00000510166.5:n.97G>T
|
|
|
ENST00000514786.1:n.48+47G>T
|
|
|
ENST00000515133.5:n.97G>T
|
|
|
ENST00000621085.4:c.56G>T
|
ENSP00000483421.1:p.Arg19Met
|
|
ENST00000621628.4:c.56G>T
|
ENSP00000480485.1:p.Arg19Met
|
|
NM_000477.5:c.56G>T
|
NP_000468.1:p.Arg19Met
|
|
NM_000477.6:c.56G>T
|
NP_000468.1:p.Arg19Met
|
|
NM_000477.7:c.56G>T
MANE Select
|
NP_000468.1:p.Arg19Met
|
|