ENST00000299314.12:c.3249G>C
MANE Select
|
ENSP00000299314.7:p.Leu1083=
|
|
ENST00000299314.11:c.3249G>C
|
ENSP00000299314.7:p.Leu1083=
|
|
ENST00000549194.1:n.115G>C
|
|
|
ENST00000550718.1:c.61G>C
|
|
|
NM_024312.4:c.3249G>C
|
NP_077288.2:p.Leu1083=
|
|
XM_006719593.2:c.3249G>C
|
XP_006719656.1:p.Leu1083=
|
|
XM_011538731.1:c.3168G>C
|
XP_011537033.1:p.Leu1056=
|
|
XM_006719593.3:c.3249G>C
|
XP_006719656.1:p.Leu1083=
|
|
XM_011538731.2:c.3168G>C
|
XP_011537033.1:p.Leu1056=
|
|
XM_017019961.1:c.3033G>C
|
XP_016875450.1:p.Leu1011=
|
|
XM_017019962.2:c.2022G>C
|
XP_016875451.1:p.Leu674=
|
|
NM_024312.5:c.3249G>C
MANE Select
|
NP_077288.2:p.Leu1083=
|
|