ENST00000642491.1:c.186+138C>T
|
ENSP00000495714.1:n.186+138C>T
|
|
ENST00000644296.1:c.186+138C>T
MANE Select
|
ENSP00000495986.1:n.186+138C>T
|
|
ENST00000240335.1:c.186+138C>T
|
ENSP00000240335.1:n.186+138C>T
|
|
ENST00000393853.8:c.186+138C>T
|
ENSP00000377435.3:n.186+138C>T
|
|
ENST00000589003.5:c.-73+138C>T
|
ENSP00000467588.1:n.-73+138C>T
|
|
NM_018488.2:c.186+138C>T
|
NP_060958.2:n.186+138C>T
|
|
XM_005257835.3:c.186+138C>T
|
XP_005257892.2:n.186+138C>T
|
|
XM_005257837.2:c.186+138C>T
|
XP_005257894.1:n.186+138C>T
|
|
XM_011525490.1:c.375+138C>T
|
XP_011523792.1:n.375+138C>T
|
|
XM_011525491.1:c.375+138C>T
|
XP_011523793.1:n.375+138C>T
|
|
XM_011525492.1:c.186+138C>T
|
XP_011523794.1:n.186+138C>T
|
|
XM_011525493.1:c.186+138C>T
|
XP_011523795.1:n.186+138C>T
|
|
XM_011525494.1:c.186+138C>T
|
XP_011523796.1:n.186+138C>T
|
|
XM_011525495.1:c.375+138C>T
|
XP_011523797.1:n.375+138C>T
|
|
NM_001321120.2:c.186+138C>T
MANE Select
|
NP_001308049.1:n.186+138C>T
|
|
NM_018488.3:c.186+138C>T
|
NP_060958.2:n.186+138C>T
|
|
XM_011525490.2:c.375+138C>T
|
XP_011523792.1:n.375+138C>T
|
|
XM_011525491.2:c.375+138C>T
|
XP_011523793.1:n.375+138C>T
|
|
XM_011525495.2:c.375+138C>T
|
XP_011523797.1:n.375+138C>T
|
|