ENST00000399503.4:c.2702C>T
MANE Select
|
ENSP00000382423.3:p.Ser901Phe
|
|
ENST00000399503.3:c.2702C>T
|
ENSP00000382423.3:p.Ser901Phe
|
|
NM_005921.1:c.2702C>T
|
NP_005912.1:p.Ser901Phe
|
|
XM_005248519.3:c.2324C>T
|
XP_005248576.2:p.Ser775Phe
|
|
XM_011543406.1:c.2447C>T
|
XP_011541708.1:p.Ser816Phe
|
|
XM_011543407.1:c.2423C>T
|
XP_011541709.1:p.Ser808Phe
|
|
XM_011543408.1:c.2702C>T
|
XP_011541710.1:p.Ser901Phe
|
|
XM_017009484.1:c.2291C>T
|
XP_016864973.1:p.Ser764Phe
|
|
XM_017009485.1:c.2213C>T
|
XP_016864974.1:p.Ser738Phe
|
|
XR_001742068.2:n.2733C>T
|
|
|
NM_005921.2:c.2702C>T
MANE Select
|
NP_005912.1:p.Ser901Phe
|
|