ENST00000299314.12:c.3557G>A
MANE Select
|
ENSP00000299314.7:p.Arg1186Lys
|
|
ENST00000299314.11:c.3557G>A
|
ENSP00000299314.7:p.Arg1186Lys
|
|
ENST00000549738.5:c.455G>A
|
ENSP00000450161.1:n.455G>A
|
|
NM_024312.4:c.3557G>A
|
NP_077288.2:p.Arg1186Lys
|
|
XM_011538731.1:c.3476G>A
|
XP_011537033.1:p.Arg1159Lys
|
|
XM_011538731.2:c.3476G>A
|
XP_011537033.1:p.Arg1159Lys
|
|
XM_017019961.1:c.3341G>A
|
XP_016875450.1:p.Arg1114Lys
|
|
XM_017019962.2:c.2330G>A
|
XP_016875451.1:p.Arg777Lys
|
|
NM_024312.5:c.3557G>A
MANE Select
|
NP_077288.2:p.Arg1186Lys
|
|