ENST00000696290.1:c.117+138C>G
MANE Select
|
ENSP00000512529.1:n.117+138C>G
|
|
ENST00000155858.10:c.117+138C>G
|
ENSP00000155858.5:n.117+138C>G
|
|
ENST00000528453.1:c.117+138C>G
|
ENSP00000436809.1:n.117+138C>G
|
|
ENST00000533060.5:c.117+138C>G
|
ENSP00000434121.1:n.117+138C>G
|
|
ENST00000533881.5:c.93+138C>G
|
ENSP00000434383.1:n.93+138C>G
|
|
NM_014555.3:c.117+138C>G
|
NP_055370.1:n.117+138C>G
|
|
XM_011520035.1:c.378+138C>G
|
XP_011518337.1:n.378+138C>G
|
|
XM_017017628.1:c.171+138C>G
|
XP_016873117.1:n.171+138C>G
|
|
NM_014555.4:c.117+138C>G
MANE Select
|
NP_055370.1:n.117+138C>G
|
|