ENST00000301305.8:c.1038G>T
MANE Select
|
ENSP00000301305.4:p.Leu346=
|
|
ENST00000276833.9:c.963G>T
|
ENSP00000276833.5:p.Leu321=
|
|
ENST00000301305.7:c.1038G>T
|
ENSP00000301305.3:p.Leu346=
|
|
NM_017767.2:c.963G>T
|
NP_060237.2:p.Leu321=
|
|
NM_130849.3:c.1038G>T
|
NP_570901.2:p.Leu346=
|
|
XM_006716599.1:c.1038G>T
|
XP_006716662.1:p.Leu346=
|
|
XM_011517153.1:c.756G>T
|
XP_011515455.1:p.Leu252=
|
|
XM_024447188.1:c.756G>T
|
XP_024302956.1:p.Leu252=
|
|
XM_024447189.1:c.756G>T
|
XP_024302957.1:p.Leu252=
|
|
NM_001374839.1:c.756G>T
|
NP_001361768.1:p.Leu252=
|
|
NM_017767.3:c.963G>T
|
NP_060237.3:p.Leu321=
|
|
NM_130849.4:c.1038G>T
MANE Select
|
NP_570901.3:p.Leu346=
|
|