ENST00000449082.3:c.3088-38G>T
MANE Select
|
ENSP00000390600.2:n.3088-38G>T
|
|
ENST00000643924.1:c.3088-41G>T
|
ENSP00000495595.1:n.3088-41G>T
|
|
ENST00000655275.1:c.3115-41G>T
|
ENSP00000499510.1:n.3115-41G>T
|
|
ENST00000449082.2:c.3088-38G>T
|
ENSP00000390600.2:n.3088-38G>T
|
|
NM_001293306.2:c.3088-41G>T
|
NP_001280235.2:n.3088-41G>T
|
|
NM_001293307.2:c.2794-38G>T
|
NP_001280236.2:n.2794-38G>T
|
|
NM_006514.3:c.3088-38G>T
|
NP_006505.3:n.3088-38G>T
|
|
XM_005265371.2:c.3097-38G>T
|
XP_005265428.1:n.3097-38G>T
|
|
XM_011533993.1:c.3097-41G>T
|
XP_011532295.1:n.3097-41G>T
|
|
XM_011533994.1:c.2803-38G>T
|
XP_011532296.1:n.2803-38G>T
|
|
XM_005265371.3:c.3097-38G>T
|
XP_005265428.1:n.3097-38G>T
|
|
XM_011533993.2:c.3097-41G>T
|
XP_011532295.1:n.3097-41G>T
|
|
XM_011533994.2:c.2803-38G>T
|
XP_011532296.1:n.2803-38G>T
|
|
NM_006514.4:c.3088-38G>T
MANE Select
|
NP_006505.4:n.3088-38G>T
|
|