ENST00000316549.11:c.1604+25987C>G
MANE Select
|
ENSP00000320246.6:n.1604+25987C>G
|
|
ENST00000316549.10:c.1604+25987C>G
|
ENSP00000320246.6:n.1604+25987C>G
|
|
NM_173653.3:c.1604+25987C>G
|
NP_775924.1:n.1604+25987C>G
|
|
XM_011512703.1:c.956+25987C>G
|
XP_011511005.1:n.956+25987C>G
|
|
XM_011512703.3:c.956+25987C>G
|
XP_011511005.1:n.956+25987C>G
|
|
XM_017006202.2:c.1711+25880C>G
|
XP_016861691.1:n.1711+25880C>G
|
|
XM_017006203.1:c.1253+25987C>G
|
XP_016861692.1:n.1253+25987C>G
|
|
NM_173653.4:c.1604+25987C>G
MANE Select
|
NP_775924.1:n.1604+25987C>G
|
|