ENST00000236959.14:c.291-137G>T
MANE Select
|
ENSP00000236959.9:n.291-137G>T
|
|
ENST00000236959.13:c.291-137G>T
|
ENSP00000236959.9:n.291-137G>T
|
|
ENST00000413174.1:c.114-137G>T
|
ENSP00000402393.1:n.114-137G>T
|
|
ENST00000427397.5:c.*341-137G>T
|
ENSP00000394317.1:n.*341-137G>T
|
|
ENST00000435675.5:c.288-137G>T
|
ENSP00000415935.1:n.288-137G>T
|
|
ENST00000443953.5:c.*388-137G>T
|
ENSP00000406792.1:n.*388-137G>T
|
|
ENST00000444305.5:c.224-137G>T
|
ENSP00000388675.1:n.224-137G>T
|
|
ENST00000488712.5:n.442-76G>T
|
|
|
NM_004044.6:c.291-137G>T
|
NP_004035.2:n.291-137G>T
|
|
XM_017004187.2:c.291-137G>T
|
XP_016859676.1:n.291-137G>T
|
|
XM_024452919.1:c.114-137G>T
|
XP_024308687.1:n.114-137G>T
|
|
NM_004044.7:c.291-137G>T
MANE Select
|
NP_004035.2:n.291-137G>T
|
|