ENST00000399503.4:c.2655G>C
MANE Select
|
ENSP00000382423.3:p.Leu885Phe
|
|
ENST00000399503.3:c.2655G>C
|
ENSP00000382423.3:p.Leu885Phe
|
|
NM_005921.1:c.2655G>C
|
NP_005912.1:p.Leu885Phe
|
|
XM_005248519.3:c.2277G>C
|
XP_005248576.2:p.Leu759Phe
|
|
XM_011543406.1:c.2400G>C
|
XP_011541708.1:p.Leu800Phe
|
|
XM_011543407.1:c.2376G>C
|
XP_011541709.1:p.Leu792Phe
|
|
XM_011543408.1:c.2655G>C
|
XP_011541710.1:p.Leu885Phe
|
|
XM_017009484.1:c.2244G>C
|
XP_016864973.1:p.Leu748Phe
|
|
XM_017009485.1:c.2166G>C
|
XP_016864974.1:p.Leu722Phe
|
|
XR_001742068.2:n.2686G>C
|
|
|
NM_005921.2:c.2655G>C
MANE Select
|
NP_005912.1:p.Leu885Phe
|
|