ENST00000295897.9:c.1460T>G
MANE Select
|
ENSP00000295897.4:p.Leu487Trp
|
|
ENST00000295897.8:c.1460T>G
|
ENSP00000295897.4:p.Leu487Trp
|
|
ENST00000401494.7:c.1115T>G
|
ENSP00000384695.3:p.Leu372Trp
|
|
ENST00000415165.6:c.884T>G
|
ENSP00000401820.2:p.Leu295Trp
|
|
ENST00000476441.6:c.*739T>G
|
ENSP00000423727.1:n.*739T>G
|
|
ENST00000486939.1:n.114T>G
|
|
|
ENST00000503124.5:c.1010T>G
|
ENSP00000421027.1:p.Leu337Trp
|
|
ENST00000505649.5:n.1007T>G
|
|
|
ENST00000509063.5:c.1460T>G
|
ENSP00000422784.1:p.Leu487Trp
|
|
ENST00000511370.1:c.993T>G
|
|
|
ENST00000621085.4:c.821T>G
|
ENSP00000483421.1:p.Leu274Trp
|
|
ENST00000621628.4:c.821T>G
|
ENSP00000480485.1:p.Leu274Trp
|
|
NM_000477.5:c.1460T>G
|
NP_000468.1:p.Leu487Trp
|
|
NM_000477.6:c.1460T>G
|
NP_000468.1:p.Leu487Trp
|
|
NM_000477.7:c.1460T>G
MANE Select
|
NP_000468.1:p.Leu487Trp
|
|