ENST00000299314.12:c.453G>C
MANE Select
|
ENSP00000299314.7:p.Leu151=
|
|
ENST00000299314.11:c.453G>C
|
ENSP00000299314.7:p.Leu151=
|
|
ENST00000549940.5:c.453G>C
|
ENSP00000449150.1:p.Leu151=
|
|
ENST00000550352.1:n.247G>C
|
|
|
ENST00000552681.1:c.87G>C
|
ENSP00000449217.1:p.Leu29=
|
|
NM_024312.4:c.453G>C
|
NP_077288.2:p.Leu151=
|
|
XM_006719593.2:c.453G>C
|
XP_006719656.1:p.Leu151=
|
|
XM_011538731.1:c.372G>C
|
XP_011537033.1:p.Leu124=
|
|
XM_006719593.3:c.453G>C
|
XP_006719656.1:p.Leu151=
|
|
XM_011538731.2:c.372G>C
|
XP_011537033.1:p.Leu124=
|
|
XM_017019961.1:c.237G>C
|
XP_016875450.1:p.Leu79=
|
|
XM_017019962.2:c.-898G>C
|
XP_016875451.1:n.-898G>C
|
|
NM_024312.5:c.453G>C
MANE Select
|
NP_077288.2:p.Leu151=
|
|