ENST00000299506.3:c.39-211G>T
MANE Select
|
ENSP00000299506.3:n.39-211G>T
|
|
ENST00000299506.2:c.39-211G>T
|
ENSP00000299506.2:n.39-211G>T
|
|
ENST00000305253.8:c.204-211G>T
|
ENSP00000305426.4:n.204-211G>T
|
|
ENST00000534099.5:c.57-211G>T
|
ENSP00000434400.1:n.57-211G>T
|
|
NM_003320.4:c.204-211G>T
|
NP_003311.2:n.204-211G>T
|
|
NM_177972.2:c.39-211G>T
|
NP_813977.1:n.39-211G>T
|
|
XM_005253109.2:c.165-211G>T
|
XP_005253166.1:n.165-211G>T
|
|
XM_011520344.1:c.75-211G>T
|
XP_011518646.1:n.75-211G>T
|
|
XM_005253109.3:c.165-211G>T
|
XP_005253166.1:n.165-211G>T
|
|
XM_011520344.2:c.75-211G>T
|
XP_011518646.1:n.75-211G>T
|
|
NM_177972.3:c.39-211G>T
MANE Select
|
NP_813977.1:n.39-211G>T
|
|
NM_003320.5:c.204-211G>T
|
NP_003311.2:n.204-211G>T
|
|