ENST00000389048.8:c.3612C>A
MANE Select
|
ENSP00000373700.3:p.Leu1204=
|
|
ENST00000431873.6:c.839C>A
|
|
|
ENST00000638605.1:n.489C>A
|
|
|
ENST00000642122.1:c.408C>A
|
ENSP00000493203.1:p.Leu136=
|
|
ENST00000389048.7:c.3612C>A
|
ENSP00000373700.3:p.Leu1204=
|
|
ENST00000431873.5:c.492C>A
|
ENSP00000414027.2:p.Leu164=
|
|
ENST00000618119.4:c.2481C>A
|
ENSP00000482733.1:p.Leu827=
|
|
NM_004304.4:c.3612C>A
|
NP_004295.2:p.Leu1204=
|
|
NM_001353765.1:c.408C>A
|
NP_001340694.1:p.Leu136=
|
|
XM_024452778.1:c.765C>A
|
XP_024308546.1:p.Leu255=
|
|
XM_024452779.1:c.408C>A
|
XP_024308547.1:p.Leu136=
|
|
NM_004304.5:c.3612C>A
MANE Select
|
NP_004295.2:p.Leu1204=
|
|
NM_001353765.2:c.408C>A
|
NP_001340694.1:p.Leu136=
|
|