ENST00000257527.9:c.666+579C>G
MANE Select
|
ENSP00000257527.5:n.666+579C>G
|
|
ENST00000257527.8:c.666+579C>G
|
ENSP00000257527.4:n.666+579C>G
|
|
ENST00000517905.1:c.666+579C>G
|
ENSP00000428654.1:n.666+579C>G
|
|
ENST00000517951.5:c.666+579C>G
|
ENSP00000428376.1:n.666+579C>G
|
|
NM_033274.4:c.666+579C>G
|
NP_150377.1:n.666+579C>G
|
|
XM_005266003.2:c.666+579C>G
|
XP_005266060.1:n.666+579C>G
|
|
XM_011534680.1:c.-135-4739C>G
|
XP_011532982.1:n.-135-4739C>G
|
|
XM_011534681.1:c.-145-4739C>G
|
XP_011532983.1:n.-145-4739C>G
|
|
NM_033274.5:c.666+579C>G
MANE Select
|
NP_150377.1:n.666+579C>G
|
|