ENST00000392666.6:c.418C>T
MANE Select
|
ENSP00000376434.1:p.Leu140=
|
|
ENST00000324003.3:c.418C>T
|
|
|
ENST00000324036.7:c.418C>T
|
ENSP00000316233.3:p.Leu140=
|
|
ENST00000392664.2:c.475C>T
|
ENSP00000376432.2:p.Leu159=
|
|
ENST00000392665.6:c.418C>T
|
ENSP00000376433.2:p.Leu140=
|
|
ENST00000392666.5:c.418C>T
|
ENSP00000376434.1:p.Leu140=
|
|
ENST00000440599.6:c.418C>T
|
ENSP00000406320.2:p.Leu140=
|
|
NM_000220.4:c.475C>T
|
NP_000211.1:p.Leu159=
|
|
NM_153764.2:c.418C>T
|
NP_722448.1:p.Leu140=
|
|
NM_153765.2:c.469C>T
|
NP_722449.3:p.Leu157=
|
|
NM_153766.2:c.418C>T
|
NP_722450.1:p.Leu140=
|
|
NM_153767.3:c.418C>T
|
NP_722451.1:p.Leu140=
|
|
NM_000220.6:c.475C>T
|
NP_000211.1:p.Leu159=
|
|
NM_153764.3:c.418C>T
|
NP_722448.1:p.Leu140=
|
|
NM_153765.3:c.469C>T
|
NP_722449.3:p.Leu157=
|
|
NM_153766.3:c.418C>T
MANE Select
|
NP_722450.1:p.Leu140=
|
|
NM_153767.4:c.418C>T
|
NP_722451.1:p.Leu140=
|
|