ENST00000322776.11:c.1024C>T
MANE Select
|
ENSP00000322450.6:p.Leu342=
|
|
ENST00000647561.1:c.1024C>T
|
ENSP00000497587.1:p.Leu342=
|
|
ENST00000322776.10:c.1024C>T
|
ENSP00000322450.6:p.Leu342=
|
|
ENST00000415352.6:c.1003C>T
|
ENSP00000395368.2:p.Leu335=
|
|
ENST00000526169.1:n.656-9C>T
|
|
|
ENST00000526770.5:n.1307C>T
|
|
|
ENST00000527355.5:c.313C>T
|
ENSP00000432637.1:p.Leu105=
|
|
ENST00000527923.1:n.366C>T
|
|
|
ENST00000529927.5:c.997C>T
|
ENSP00000436766.1:p.Leu333=
|
|
ENST00000532303.5:c.721C>T
|
ENSP00000432015.1:p.Leu241=
|
|
ENST00000533919.5:c.428C>T
|
ENSP00000435199.1:n.428C>T
|
|
NM_001166102.1:c.997C>T
|
NP_001159574.1:p.Leu333=
|
|
NM_007103.3:c.1024C>T
|
NP_009034.2:p.Leu342=
|
|
NM_001166102.2:c.997C>T
|
NP_001159574.1:p.Leu333=
|
|
NM_007103.4:c.1024C>T
MANE Select
|
NP_009034.2:p.Leu342=
|
|