ENST00000624552.4:c.14936A>G
|
ENSP00000485357.2:p.His4979Arg
|
|
ENST00000683500.2:c.14993A>G
MANE Select
|
ENSP00000508292.2:p.His4998Arg
|
|
ENST00000623487.1:n.3339A>G
|
|
|
ENST00000624552.3:c.14933A>G
|
ENSP00000485357.1:p.His4978Arg
|
|
NM_001291815.1:c.14993A>G
|
NP_001278744.1:p.His4998Arg
|
|
XM_011518465.1:c.14870A>G
|
XP_011516767.1:p.His4957Arg
|
|
XM_011518466.1:c.14861A>G
|
XP_011516768.1:p.His4954Arg
|
|
XM_011518467.1:c.14816A>G
|
XP_011516769.1:p.His4939Arg
|
|
NM_001291815.2:c.14993A>G
MANE Select
|
NP_001278744.1:p.His4998Arg
|
|
XM_011518465.2:c.14870A>G
|
XP_011516767.1:p.His4957Arg
|
|
XM_011518466.2:c.14861A>G
|
XP_011516768.1:p.His4954Arg
|
|
XM_011518467.2:c.14816A>G
|
XP_011516769.1:p.His4939Arg
|
|
XM_017014585.1:c.11774A>G
|
XP_016870074.1:p.His3925Arg
|
|
XM_017014586.1:c.7571A>G
|
XP_016870075.1:p.His2524Arg
|
|
XR_001746957.1:n.92+175T>C
|
|
|
XR_001746958.1:n.92+175T>C
|
|
|