ENST00000258428.8:c.770T>C
MANE Select
|
ENSP00000258428.3:p.Phe257Ser
|
|
ENST00000258428.7:c.770T>C
|
ENSP00000258428.3:p.Phe257Ser
|
|
ENST00000393445.7:c.770T>C
|
ENSP00000377091.3:p.Phe257Ser
|
|
ENST00000413697.5:c.*717T>C
|
ENSP00000416274.1:n.*717T>C
|
|
ENST00000465835.5:n.725T>C
|
|
|
ENST00000473819.1:n.882T>C
|
|
|
NM_001037872.1:c.770T>C
|
NP_001032961.1:p.Phe257Ser
|
|
NM_016316.2:c.770T>C
|
NP_057400.1:p.Phe257Ser
|
|
XM_011511336.1:c.770T>C
|
XP_011509638.1:p.Phe257Ser
|
|
XM_011511337.1:c.770T>C
|
XP_011509639.1:p.Phe257Ser
|
|
XM_011511338.1:c.560T>C
|
XP_011509640.1:p.Phe187Ser
|
|
XR_427092.1:n.1151T>C
|
|
|
XR_922941.1:n.780T>C
|
|
|
NM_001037872.2:c.770T>C
|
NP_001032961.1:p.Phe257Ser
|
|
NM_001321454.1:c.770T>C
|
NP_001308383.1:p.Phe257Ser
|
|
NM_001321455.1:c.560T>C
|
NP_001308384.1:p.Phe187Ser
|
|
NM_001321458.1:c.-825T>C
|
NP_001308387.1:n.-825T>C
|
|
NM_001321459.1:c.-1000T>C
|
NP_001308388.1:n.-1000T>C
|
|
NM_001321460.1:c.-997T>C
|
NP_001308389.1:n.-997T>C
|
|
NM_016316.3:c.770T>C
|
NP_057400.1:p.Phe257Ser
|
|
NR_135649.1:n.1020T>C
|
|
|
NR_135650.1:n.1177T>C
|
|
|
NR_135651.1:n.1020T>C
|
|
|
NR_135652.1:n.1020T>C
|
|
|
NR_135653.1:n.1020T>C
|
|
|
XM_017004309.2:c.800T>C
|
XP_016859798.1:p.Phe267Ser
|
|
XM_017004310.1:c.770T>C
|
XP_016859799.1:p.Phe257Ser
|
|
XM_017004311.1:c.770T>C
|
XP_016859800.1:p.Phe257Ser
|
|
XM_017004312.2:c.770T>C
|
XP_016859801.1:p.Phe257Ser
|
|
XM_017004313.1:c.1094T>C
|
XP_016859802.1:p.Phe365Ser
|
|
XM_017004314.2:c.-1025T>C
|
XP_016859803.1:n.-1025T>C
|
|
XM_017004315.2:c.-1018T>C
|
XP_016859804.1:n.-1018T>C
|
|
XM_024452960.1:c.-1616T>C
|
XP_024308728.1:n.-1616T>C
|
|
NM_016316.4:c.770T>C
MANE Select
|
NP_057400.1:p.Phe257Ser
|
|
NM_001037872.3:c.770T>C
|
NP_001032961.1:p.Phe257Ser
|
|
NM_001321454.2:c.770T>C
|
NP_001308383.1:p.Phe257Ser
|
|
NM_001321455.2:c.560T>C
|
NP_001308384.1:p.Phe187Ser
|
|
NM_001321458.2:c.-825T>C
|
NP_001308387.1:n.-825T>C
|
|
NM_001321459.2:c.-1000T>C
|
NP_001308388.1:n.-1000T>C
|
|
NM_001321460.2:c.-997T>C
|
NP_001308389.1:n.-997T>C
|
|
NR_135649.2:n.981T>C
|
|
|
NR_135650.2:n.1138T>C
|
|
|
NR_135651.2:n.981T>C
|
|
|
NR_135652.2:n.981T>C
|
|
|
NR_135653.2:n.981T>C
|
|
|