ENST00000295897.9:c.271C>G
MANE Select
|
ENSP00000295897.4:p.His91Asp
|
|
ENST00000295897.8:c.271C>G
|
ENSP00000295897.4:p.His91Asp
|
|
ENST00000401494.7:c.138-761C>G
|
ENSP00000384695.3:n.138-761C>G
|
|
ENST00000415165.6:c.138-3402C>G
|
ENSP00000401820.2:n.138-3402C>G
|
|
ENST00000441319.5:c.277C>G
|
ENSP00000392541.1:p.His93Asp
|
|
ENST00000476441.6:c.80-761C>G
|
ENSP00000423727.1:n.80-761C>G
|
|
ENST00000503124.5:c.33-761C>G
|
ENSP00000421027.1:n.33-761C>G
|
|
ENST00000509063.5:c.271C>G
|
ENSP00000422784.1:p.His91Asp
|
|
ENST00000510166.5:n.307C>G
|
|
|
ENST00000514786.1:n.240C>G
|
|
|
ENST00000515133.5:n.312C>G
|
|
|
ENST00000621085.4:c.271C>G
|
ENSP00000483421.1:p.His91Asp
|
|
ENST00000621628.4:c.271C>G
|
ENSP00000480485.1:p.His91Asp
|
|
NM_000477.5:c.271C>G
|
NP_000468.1:p.His91Asp
|
|
NM_000477.6:c.271C>G
|
NP_000468.1:p.His91Asp
|
|
NM_000477.7:c.271C>G
MANE Select
|
NP_000468.1:p.His91Asp
|
|