ENST00000236959.14:c.369A>C
MANE Select
|
ENSP00000236959.9:p.Gln123His
|
|
ENST00000236959.13:c.369A>C
|
ENSP00000236959.9:p.Gln123His
|
|
ENST00000413174.1:c.192A>C
|
ENSP00000402393.1:p.Gln64His
|
|
ENST00000427397.5:c.*419A>C
|
ENSP00000394317.1:n.*419A>C
|
|
ENST00000435675.5:c.366A>C
|
ENSP00000415935.1:p.Gln122His
|
|
ENST00000443953.5:c.*466A>C
|
ENSP00000406792.1:n.*466A>C
|
|
ENST00000444305.5:c.*47A>C
|
ENSP00000388675.1:n.*47A>C
|
|
ENST00000488712.5:n.581A>C
|
|
|
NM_004044.6:c.369A>C
|
NP_004035.2:p.Gln123His
|
|
XM_017004187.2:c.369A>C
|
XP_016859676.1:p.Gln123His
|
|
XM_024452919.1:c.192A>C
|
XP_024308687.1:p.Gln64His
|
|
NM_004044.7:c.369A>C
MANE Select
|
NP_004035.2:p.Gln123His
|
|