ENST00000624552.4:c.14937C>A
|
ENSP00000485357.2:p.His4979Gln
|
|
ENST00000683500.2:c.14994C>A
MANE Select
|
ENSP00000508292.2:p.His4998Gln
|
|
ENST00000623487.1:n.3340C>A
|
|
|
ENST00000624552.3:c.14934C>A
|
ENSP00000485357.1:p.His4978Gln
|
|
NM_001291815.1:c.14994C>A
|
NP_001278744.1:p.His4998Gln
|
|
XM_011518465.1:c.14871C>A
|
XP_011516767.1:p.His4957Gln
|
|
XM_011518466.1:c.14862C>A
|
XP_011516768.1:p.His4954Gln
|
|
XM_011518467.1:c.14817C>A
|
XP_011516769.1:p.His4939Gln
|
|
NM_001291815.2:c.14994C>A
MANE Select
|
NP_001278744.1:p.His4998Gln
|
|
XM_011518465.2:c.14871C>A
|
XP_011516767.1:p.His4957Gln
|
|
XM_011518466.2:c.14862C>A
|
XP_011516768.1:p.His4954Gln
|
|
XM_011518467.2:c.14817C>A
|
XP_011516769.1:p.His4939Gln
|
|
XM_017014585.1:c.11775C>A
|
XP_016870074.1:p.His3925Gln
|
|
XM_017014586.1:c.7572C>A
|
XP_016870075.1:p.His2524Gln
|
|
XR_001746957.1:n.92+174G>T
|
|
|
XR_001746958.1:n.92+174G>T
|
|
|