ENST00000295897.9:c.512C>G
MANE Select
|
ENSP00000295897.4:p.Pro171Arg
|
|
ENST00000295897.8:c.512C>G
|
ENSP00000295897.4:p.Pro171Arg
|
|
ENST00000401494.7:c.167C>G
|
ENSP00000384695.3:p.Pro56Arg
|
|
ENST00000415165.6:c.138-2612C>G
|
ENSP00000401820.2:n.138-2612C>G
|
|
ENST00000441319.5:c.518C>G
|
ENSP00000392541.1:p.Pro173Arg
|
|
ENST00000476441.6:c.109C>G
|
ENSP00000423727.1:p.Leu37Val
|
|
ENST00000503124.5:c.62C>G
|
ENSP00000421027.1:p.Pro21Arg
|
|
ENST00000505649.5:n.198C>G
|
|
|
ENST00000509063.5:c.512C>G
|
ENSP00000422784.1:p.Pro171Arg
|
|
ENST00000511370.1:c.45C>G
|
|
|
ENST00000514786.1:n.481C>G
|
|
|
ENST00000621085.4:c.490+22C>G
|
ENSP00000483421.1:n.490+22C>G
|
|
ENST00000621628.4:c.486+308C>G
|
ENSP00000480485.1:n.486+308C>G
|
|
NM_000477.5:c.512C>G
|
NP_000468.1:p.Pro171Arg
|
|
NM_000477.6:c.512C>G
|
NP_000468.1:p.Pro171Arg
|
|
NM_000477.7:c.512C>G
MANE Select
|
NP_000468.1:p.Pro171Arg
|
|