ENST00000361915.8:c.3701-169C>T
MANE Select
|
ENSP00000355106.3:n.3701-169C>T
|
|
ENST00000637337.1:n.3912-169C>T
|
|
|
ENST00000294724.8:c.3701-169C>T
|
ENSP00000294724.4:n.3701-169C>T
|
|
ENST00000361302.7:c.3653-169C>T
|
ENSP00000354971.3:n.3653-169C>T
|
|
ENST00000361522.4:c.3650-169C>T
|
ENSP00000354635.4:n.3650-169C>T
|
|
ENST00000361915.7:c.3701-169C>T
|
ENSP00000355106.3:n.3701-169C>T
|
|
ENST00000370161.6:c.3653-169C>T
|
ENSP00000359180.2:n.3653-169C>T
|
|
ENST00000370163.7:c.3701-169C>T
|
ENSP00000359182.3:n.3701-169C>T
|
|
ENST00000370165.7:c.3701-169C>T
|
ENSP00000359184.3:n.3701-169C>T
|
|
NM_000028.2:c.3701-169C>T
|
NP_000019.2:n.3701-169C>T
|
|
NM_000642.2:c.3701-169C>T
|
NP_000633.2:n.3701-169C>T
|
|
NM_000643.2:c.3701-169C>T
|
NP_000634.2:n.3701-169C>T
|
|
NM_000644.2:c.3701-169C>T
|
NP_000635.2:n.3701-169C>T
|
|
NM_000645.2:c.3650-169C>T
|
NP_000636.2:n.3650-169C>T
|
|
NM_000646.2:c.3653-169C>T
|
NP_000637.2:n.3653-169C>T
|
|
XM_005270557.1:c.3701-169C>T
|
XP_005270614.1:n.3701-169C>T
|
|
XM_005270557.2:c.3701-169C>T
|
XP_005270614.1:n.3701-169C>T
|
|
XM_017000501.2:c.1961-169C>T
|
XP_016855990.1:n.1961-169C>T
|
|
NM_000642.3:c.3701-169C>T
MANE Select
|
NP_000633.2:n.3701-169C>T
|
|