ENST00000236959.14:c.815-102T>A
MANE Select
|
ENSP00000236959.9:n.815-102T>A
|
|
ENST00000236959.13:c.815-102T>A
|
ENSP00000236959.9:n.815-102T>A
|
|
ENST00000427397.5:c.*708-102T>A
|
ENSP00000394317.1:n.*708-102T>A
|
|
ENST00000435675.5:c.812-102T>A
|
ENSP00000415935.1:n.812-102T>A
|
|
ENST00000443953.5:c.*912-102T>A
|
ENSP00000406792.1:n.*912-102T>A
|
|
NM_004044.6:c.815-102T>A
|
NP_004035.2:n.815-102T>A
|
|
XM_017004187.2:c.815-102T>A
|
XP_016859676.1:n.815-102T>A
|
|
XM_024452919.1:c.638-102T>A
|
XP_024308687.1:n.638-102T>A
|
|
NM_004044.7:c.815-102T>A
MANE Select
|
NP_004035.2:n.815-102T>A
|
|