ENST00000624552.4:c.14959T>G
|
ENSP00000485357.2:p.Phe4987Val
|
|
ENST00000683500.2:c.15016T>G
MANE Select
|
ENSP00000508292.2:p.Phe5006Val
|
|
ENST00000623487.1:n.3362T>G
|
|
|
ENST00000624552.3:c.14956T>G
|
ENSP00000485357.1:p.Phe4986Val
|
|
NM_001291815.1:c.15016T>G
|
NP_001278744.1:p.Phe5006Val
|
|
XM_011518465.1:c.14893T>G
|
XP_011516767.1:p.Phe4965Val
|
|
XM_011518466.1:c.14884T>G
|
XP_011516768.1:p.Phe4962Val
|
|
XM_011518467.1:c.14839T>G
|
XP_011516769.1:p.Phe4947Val
|
|
NM_001291815.2:c.15016T>G
MANE Select
|
NP_001278744.1:p.Phe5006Val
|
|
XM_011518465.2:c.14893T>G
|
XP_011516767.1:p.Phe4965Val
|
|
XM_011518466.2:c.14884T>G
|
XP_011516768.1:p.Phe4962Val
|
|
XM_011518467.2:c.14839T>G
|
XP_011516769.1:p.Phe4947Val
|
|
XM_017014585.1:c.11797T>G
|
XP_016870074.1:p.Phe3933Val
|
|
XM_017014586.1:c.7594T>G
|
XP_016870075.1:p.Phe2532Val
|
|
XR_001746957.1:n.92+152A>C
|
|
|
XR_001746958.1:n.92+152A>C
|
|
|