ENST00000624552.4:c.14960T>C
|
ENSP00000485357.2:p.Phe4987Ser
|
|
ENST00000683500.2:c.15017T>C
MANE Select
|
ENSP00000508292.2:p.Phe5006Ser
|
|
ENST00000623487.1:n.3363T>C
|
|
|
ENST00000624552.3:c.14957T>C
|
ENSP00000485357.1:p.Phe4986Ser
|
|
NM_001291815.1:c.15017T>C
|
NP_001278744.1:p.Phe5006Ser
|
|
XM_011518465.1:c.14894T>C
|
XP_011516767.1:p.Phe4965Ser
|
|
XM_011518466.1:c.14885T>C
|
XP_011516768.1:p.Phe4962Ser
|
|
XM_011518467.1:c.14840T>C
|
XP_011516769.1:p.Phe4947Ser
|
|
NM_001291815.2:c.15017T>C
MANE Select
|
NP_001278744.1:p.Phe5006Ser
|
|
XM_011518465.2:c.14894T>C
|
XP_011516767.1:p.Phe4965Ser
|
|
XM_011518466.2:c.14885T>C
|
XP_011516768.1:p.Phe4962Ser
|
|
XM_011518467.2:c.14840T>C
|
XP_011516769.1:p.Phe4947Ser
|
|
XM_017014585.1:c.11798T>C
|
XP_016870074.1:p.Phe3933Ser
|
|
XM_017014586.1:c.7595T>C
|
XP_016870075.1:p.Phe2532Ser
|
|
XR_001746957.1:n.92+151A>G
|
|
|
XR_001746958.1:n.92+151A>G
|
|
|