ENST00000381334.10:c.793-577C>G
MANE Select
|
ENSP00000370736.5:n.793-577C>G
|
|
ENST00000381334.9:c.793-577C>G
|
ENSP00000370736.5:n.793-577C>G
|
|
ENST00000506103.2:c.247-577C>G
|
|
|
ENST00000506198.5:c.208-577C>G
|
ENSP00000425449.1:n.208-577C>G
|
|
ENST00000508404.5:c.*665-577C>G
|
ENSP00000422639.1:n.*665-577C>G
|
|
ENST00000508561.5:n.489-577C>G
|
|
|
ENST00000509575.1:n.296-577C>G
|
|
|
ENST00000514904.5:n.1247-577C>G
|
|
|
ENST00000515591.1:n.848C>G
|
|
|
ENST00000608091.1:c.303-577C>G
|
|
|
NM_018475.4:c.793-577C>G
|
NP_060945.2:n.793-577C>G
|
|
NR_073070.1:n.1173-577C>G
|
|
|
XM_011534394.1:c.793-577C>G
|
XP_011532696.1:n.793-577C>G
|
|
XM_011534394.3:c.793-577C>G
|
XP_011532696.1:n.793-577C>G
|
|
XM_017008412.1:c.604-577C>G
|
XP_016863901.1:n.604-577C>G
|
|
XR_001741287.2:n.1509-577C>G
|
|
|
NM_018475.5:c.793-577C>G
MANE Select
|
NP_060945.2:n.793-577C>G
|
|
NR_073070.2:n.1129-577C>G
|
|
|