ENST00000375448.4:c.340+197A>T
MANE Select
|
ENSP00000364597.4:n.340+197A>T
|
|
ENST00000375453.5:c.341-118A>T
|
ENSP00000364602.1:n.341-118A>T
|
|
NM_012387.2:c.340+197A>T
|
NP_036519.2:n.340+197A>T
|
|
XM_011541150.1:c.340+197A>T
|
XP_011539452.1:n.340+197A>T
|
|
XM_011541151.1:c.340+197A>T
|
XP_011539453.1:n.340+197A>T
|
|
XM_011541152.1:c.-80+197A>T
|
XP_011539454.1:n.-80+197A>T
|
|
XM_011541153.1:c.340+197A>T
|
XP_011539455.1:n.340+197A>T
|
|
XM_011541154.1:c.340+197A>T
|
XP_011539456.1:n.340+197A>T
|
|
XM_011541155.1:c.340+197A>T
|
XP_011539457.1:n.340+197A>T
|
|
XM_011541156.1:c.340+197A>T
|
XP_011539458.1:n.340+197A>T
|
|
XM_011541157.1:c.-373+197A>T
|
XP_011539459.1:n.-373+197A>T
|
|
XM_011541154.2:c.340+197A>T
|
XP_011539456.1:n.340+197A>T
|
|
NM_012387.3:c.340+197A>T
MANE Select
|
NP_036519.2:n.340+197A>T
|
|