ENST00000350721.9:c.6283C>T
MANE Select
|
ENSP00000343741.4:p.Leu2095Phe
|
|
ENST00000513291.2:n.1467C>T
|
|
|
ENST00000654170.1:n.1126C>T
|
|
|
ENST00000656590.1:c.5073C>T
|
|
|
ENST00000661310.1:c.6091C>T
|
ENSP00000499589.1:p.Leu2031Phe
|
|
ENST00000665483.1:n.138C>T
|
|
|
ENST00000666447.1:n.118C>T
|
|
|
ENST00000666943.1:n.1747C>T
|
|
|
ENST00000350721.8:c.6283C>T
|
ENSP00000343741.4:p.Leu2095Phe
|
|
NM_001184.3:c.6283C>T
|
NP_001175.2:p.Leu2095Phe
|
|
XM_011512924.1:c.6289C>T
|
XP_011511226.1:p.Leu2097Phe
|
|
XM_011512925.1:c.6097C>T
|
XP_011511227.1:p.Leu2033Phe
|
|
XR_924147.1:n.6378C>T
|
|
|
XR_924148.1:n.6378C>T
|
|
|
XR_924149.1:n.6257C>T
|
|
|
NM_001354579.1:c.6091C>T
|
NP_001341508.1:p.Leu2031Phe
|
|
XR_001740179.2:n.6372C>T
|
|
|
XR_001740180.2:n.6426C>T
|
|
|
XR_001740181.2:n.6305C>T
|
|
|
XR_001740182.1:n.6257C>T
|
|
|
XR_002959543.1:n.6482C>T
|
|
|
XR_924148.2:n.6378C>T
|
|
|
NM_001184.4:c.6283C>T
MANE Select
|
NP_001175.2:p.Leu2095Phe
|
|
NM_001354579.2:c.6091C>T
|
NP_001341508.1:p.Leu2031Phe
|
|