ENST00000350721.9:c.6245T>C
MANE Select
|
ENSP00000343741.4:p.Phe2082Ser
|
|
ENST00000513291.2:n.1429T>C
|
|
|
ENST00000654170.1:n.1088T>C
|
|
|
ENST00000656590.1:c.5035T>C
|
|
|
ENST00000661310.1:c.6053T>C
|
ENSP00000499589.1:p.Phe2018Ser
|
|
ENST00000665483.1:n.100T>C
|
|
|
ENST00000666447.1:n.80T>C
|
|
|
ENST00000666943.1:n.1709T>C
|
|
|
ENST00000350721.8:c.6245T>C
|
ENSP00000343741.4:p.Phe2082Ser
|
|
NM_001184.3:c.6245T>C
|
NP_001175.2:p.Phe2082Ser
|
|
XM_011512924.1:c.6251T>C
|
XP_011511226.1:p.Phe2084Ser
|
|
XM_011512925.1:c.6059T>C
|
XP_011511227.1:p.Phe2020Ser
|
|
XR_924147.1:n.6340T>C
|
|
|
XR_924148.1:n.6340T>C
|
|
|
XR_924149.1:n.6219T>C
|
|
|
NM_001354579.1:c.6053T>C
|
NP_001341508.1:p.Phe2018Ser
|
|
XR_001740179.2:n.6334T>C
|
|
|
XR_001740180.2:n.6388T>C
|
|
|
XR_001740181.2:n.6267T>C
|
|
|
XR_001740182.1:n.6219T>C
|
|
|
XR_002959543.1:n.6444T>C
|
|
|
XR_924148.2:n.6340T>C
|
|
|
NM_001184.4:c.6245T>C
MANE Select
|
NP_001175.2:p.Phe2082Ser
|
|
NM_001354579.2:c.6053T>C
|
NP_001341508.1:p.Phe2018Ser
|
|