ENST00000260408.8:c.1804+186A>T
MANE Select
|
ENSP00000260408.3:n.1804+186A>T
|
|
ENST00000260408.7:c.1804+186A>T
|
ENSP00000260408.3:n.1804+186A>T
|
|
ENST00000396136.6:c.1630+186A>T
|
|
|
ENST00000402627.5:c.155-13295A>T
|
ENSP00000386056.1:n.155-13295A>T
|
|
ENST00000470269.5:n.333+186A>T
|
|
|
ENST00000482945.5:n.1213A>T
|
|
|
ENST00000561288.1:c.56-13295A>T
|
ENSP00000452639.1:n.56-13295A>T
|
|
NM_001110.3:c.1804+186A>T
|
NP_001101.1:n.1804+186A>T
|
|
XM_005254117.2:c.1711+186A>T
|
XP_005254174.1:n.1711+186A>T
|
|
NM_001320570.1:c.1711+186A>T
|
NP_001307499.1:n.1711+186A>T
|
|
XM_024449818.1:c.1582+186A>T
|
XP_024305586.1:n.1582+186A>T
|
|
NM_001110.4:c.1804+186A>T
MANE Select
|
NP_001101.1:n.1804+186A>T
|
|
NM_001320570.2:c.1711+186A>T
|
NP_001307499.1:n.1711+186A>T
|
|