ENST00000372348.9:c.1142+40G>T
|
ENSP00000361423.2:n.1142+40G>T
|
|
ENST00000318560.6:c.1085+40G>T
MANE Select
|
ENSP00000323315.5:n.1085+40G>T
|
|
ENST00000372348.7:c.1142+40G>T
|
ENSP00000361423.2:n.1142+40G>T
|
|
ENST00000318560.5:c.1085+40G>T
|
ENSP00000323315.5:n.1085+40G>T
|
|
ENST00000372348.6:c.1142+40G>T
|
ENSP00000361423.2:n.1142+40G>T
|
|
NM_005157.5:c.1085+40G>T
|
NP_005148.2:n.1085+40G>T
|
|
NM_007313.2:c.1142+40G>T
|
NP_009297.2:n.1142+40G>T
|
|
NM_005157.6:c.1085+40G>T
MANE Select
|
NP_005148.2:n.1085+40G>T
|
|
NM_007313.3:c.1142+40G>T
|
NP_009297.2:n.1142+40G>T
|
|