ENST00000299506.3:c.90+56G>T
MANE Select
|
ENSP00000299506.3:n.90+56G>T
|
|
ENST00000299506.2:c.90+56G>T
|
ENSP00000299506.2:n.90+56G>T
|
|
ENST00000305253.8:c.255+56G>T
|
ENSP00000305426.4:n.255+56G>T
|
|
ENST00000534099.5:c.108+56G>T
|
ENSP00000434400.1:n.108+56G>T
|
|
NM_003320.4:c.255+56G>T
|
NP_003311.2:n.255+56G>T
|
|
NM_177972.2:c.90+56G>T
|
NP_813977.1:n.90+56G>T
|
|
XM_005253109.2:c.216+56G>T
|
XP_005253166.1:n.216+56G>T
|
|
XM_011520344.1:c.126+56G>T
|
XP_011518646.1:n.126+56G>T
|
|
XM_005253109.3:c.216+56G>T
|
XP_005253166.1:n.216+56G>T
|
|
XM_011520344.2:c.126+56G>T
|
XP_011518646.1:n.126+56G>T
|
|
NM_177972.3:c.90+56G>T
MANE Select
|
NP_813977.1:n.90+56G>T
|
|
NM_003320.5:c.255+56G>T
|
NP_003311.2:n.255+56G>T
|
|