ENST00000442544.7:c.1861+144T>A
MANE Select
|
ENSP00000389140.2:n.1861+144T>A
|
|
ENST00000304775.12:c.1662+144T>A
|
|
|
ENST00000412726.5:c.1792+144T>A
|
ENSP00000397322.2:n.1792+144T>A
|
|
ENST00000442544.6:c.1861+144T>A
|
ENSP00000389140.2:n.1861+144T>A
|
|
ENST00000581580.5:c.826+144T>A
|
ENSP00000464582.1:n.826+144T>A
|
|
NM_005215.3:c.1861+144T>A
|
NP_005206.2:n.1861+144T>A
|
|
XM_011525843.1:c.1861+144T>A
|
XP_011524145.1:n.1861+144T>A
|
|
XM_011525844.1:c.826+144T>A
|
XP_011524146.1:n.826+144T>A
|
|
XM_011525845.1:c.1861+144T>A
|
XP_011524147.1:n.1861+144T>A
|
|
XM_011525846.1:c.1861+144T>A
|
XP_011524148.1:n.1861+144T>A
|
|
XM_011525844.2:c.826+144T>A
|
XP_011524146.1:n.826+144T>A
|
|
XM_017025568.1:c.1861+144T>A
|
XP_016881057.1:n.1861+144T>A
|
|
XM_017025569.1:c.1861+144T>A
|
XP_016881058.1:n.1861+144T>A
|
|
XM_017025570.1:c.826+144T>A
|
XP_016881059.1:n.826+144T>A
|
|
NM_005215.4:c.1861+144T>A
MANE Select
|
NP_005206.2:n.1861+144T>A
|
|