ENST00000350721.9:c.6225T>G
MANE Select
|
ENSP00000343741.4:p.Ser2075=
|
|
ENST00000513291.2:n.1409T>G
|
|
|
ENST00000654170.1:n.1068T>G
|
|
|
ENST00000656590.1:c.5015T>G
|
|
|
ENST00000661310.1:c.6033T>G
|
ENSP00000499589.1:p.Ser2011=
|
|
ENST00000665483.1:n.80T>G
|
|
|
ENST00000666447.1:n.60T>G
|
|
|
ENST00000666943.1:n.1689T>G
|
|
|
ENST00000350721.8:c.6225T>G
|
ENSP00000343741.4:p.Ser2075=
|
|
NM_001184.3:c.6225T>G
|
NP_001175.2:p.Ser2075=
|
|
XM_011512924.1:c.6231T>G
|
XP_011511226.1:p.Ser2077=
|
|
XM_011512925.1:c.6039T>G
|
XP_011511227.1:p.Ser2013=
|
|
XR_924147.1:n.6320T>G
|
|
|
XR_924148.1:n.6320T>G
|
|
|
XR_924149.1:n.6199T>G
|
|
|
NM_001354579.1:c.6033T>G
|
NP_001341508.1:p.Ser2011=
|
|
XR_001740179.2:n.6314T>G
|
|
|
XR_001740180.2:n.6368T>G
|
|
|
XR_001740181.2:n.6247T>G
|
|
|
XR_001740182.1:n.6199T>G
|
|
|
XR_002959543.1:n.6424T>G
|
|
|
XR_924148.2:n.6320T>G
|
|
|
NM_001184.4:c.6225T>G
MANE Select
|
NP_001175.2:p.Ser2075=
|
|
NM_001354579.2:c.6033T>G
|
NP_001341508.1:p.Ser2011=
|
|