ENST00000299506.3:c.99G>C
MANE Select
|
ENSP00000299506.3:p.Leu33=
|
|
ENST00000299506.2:c.99G>C
|
ENSP00000299506.2:p.Leu33=
|
|
ENST00000305253.8:c.264G>C
|
ENSP00000305426.4:p.Leu88=
|
|
ENST00000534099.5:c.117G>C
|
ENSP00000434400.1:p.Leu39=
|
|
NM_003320.4:c.264G>C
|
NP_003311.2:p.Leu88=
|
|
NM_177972.2:c.99G>C
|
NP_813977.1:p.Leu33=
|
|
XM_005253109.2:c.225G>C
|
XP_005253166.1:p.Leu75=
|
|
XM_011520344.1:c.135G>C
|
XP_011518646.1:p.Leu45=
|
|
XM_005253109.3:c.225G>C
|
XP_005253166.1:p.Leu75=
|
|
XM_011520344.2:c.135G>C
|
XP_011518646.1:p.Leu45=
|
|
NM_177972.3:c.99G>C
MANE Select
|
NP_813977.1:p.Leu33=
|
|
NM_003320.5:c.264G>C
|
NP_003311.2:p.Leu88=
|
|