ENST00000624552.4:c.14935C>G
|
ENSP00000485357.2:p.His4979Asp
|
|
ENST00000683500.2:c.14992C>G
MANE Select
|
ENSP00000508292.2:p.His4998Asp
|
|
ENST00000623487.1:n.3338C>G
|
|
|
ENST00000624552.3:c.14932C>G
|
ENSP00000485357.1:p.His4978Asp
|
|
NM_001291815.1:c.14992C>G
|
NP_001278744.1:p.His4998Asp
|
|
XM_011518465.1:c.14869C>G
|
XP_011516767.1:p.His4957Asp
|
|
XM_011518466.1:c.14860C>G
|
XP_011516768.1:p.His4954Asp
|
|
XM_011518467.1:c.14815C>G
|
XP_011516769.1:p.His4939Asp
|
|
NM_001291815.2:c.14992C>G
MANE Select
|
NP_001278744.1:p.His4998Asp
|
|
XM_011518465.2:c.14869C>G
|
XP_011516767.1:p.His4957Asp
|
|
XM_011518466.2:c.14860C>G
|
XP_011516768.1:p.His4954Asp
|
|
XM_011518467.2:c.14815C>G
|
XP_011516769.1:p.His4939Asp
|
|
XM_017014585.1:c.11773C>G
|
XP_016870074.1:p.His3925Asp
|
|
XM_017014586.1:c.7570C>G
|
XP_016870075.1:p.His2524Asp
|
|
XR_001746957.1:n.92+176G>C
|
|
|
XR_001746958.1:n.92+176G>C
|
|
|