ENST00000338508.9:c.2422G>T
|
ENSP00000345193.7:p.Ala808Ser
|
|
ENST00000412252.6:c.757+4199G>T
|
ENSP00000414876.2:n.757+4199G>T
|
|
ENST00000601538.6:c.4189G>T
MANE Select
|
ENSP00000469689.2:p.Ala1397Ser
|
|
ENST00000654939.1:c.1617G>T
|
|
|
ENST00000656230.1:c.3052G>T
|
ENSP00000499561.1:p.Ala1018Ser
|
|
ENST00000659264.1:c.2479G>T
|
ENSP00000499270.1:p.Ala827Ser
|
|
ENST00000338508.8:c.2425G>T
|
ENSP00000345193.6:p.Ala809Ser
|
|
ENST00000357171.7:c.718+4199G>T
|
ENSP00000349694.4:n.718+4199G>T
|
|
ENST00000409161.5:c.2401G>T
|
ENSP00000386491.1:p.Ala801Ser
|
|
ENST00000412252.5:c.755+4199G>T
|
|
|
ENST00000423696.6:c.3052G>T
|
ENSP00000394536.2:p.Ala1018Ser
|
|
ENST00000424924.5:c.2026G>T
|
ENSP00000402944.1:p.Ala676Ser
|
|
ENST00000449833.6:c.2425G>T
|
ENSP00000399423.3:p.Ala809Ser
|
|
ENST00000601538.5:c.4189G>T
|
ENSP00000469689.2:p.Ala1397Ser
|
|
NM_012309.4:c.4189G>T
|
NP_036441.2:p.Ala1397Ser
|
|
NM_133266.4:c.2425G>T
|
NP_573573.2:p.Ala809Ser
|
|
NR_110766.1:n.833+4199G>T
|
|
|
XM_005277930.2:c.4189G>T
|
XP_005277987.1:p.Ala1397Ser
|
|
XM_005277932.2:c.3052G>T
|
XP_005277989.1:p.Ala1018Ser
|
|
XM_006718478.2:c.4159G>T
|
XP_006718541.1:p.Ala1387Ser
|
|
XM_011544854.1:c.4201G>T
|
XP_011543156.1:p.Ala1401Ser
|
|
XM_011544855.1:c.4180G>T
|
XP_011543157.1:p.Ala1394Ser
|
|
XM_011544856.1:c.4174G>T
|
XP_011543158.1:p.Ala1392Ser
|
|
XM_011544857.1:c.4153G>T
|
XP_011543159.1:p.Ala1385Ser
|
|
XM_011544858.1:c.4201G>T
|
XP_011543160.1:p.Ala1401Ser
|
|
XM_011544859.1:c.3064G>T
|
XP_011543161.1:p.Ala1022Ser
|
|
XM_005277932.3:c.3052G>T
|
XP_005277989.1:p.Ala1018Ser
|
|
XM_017017387.1:c.4189G>T
|
XP_016872876.1:p.Ala1397Ser
|
|
XM_017017388.1:c.4189G>T
|
XP_016872877.1:p.Ala1397Ser
|
|
XM_017017389.1:c.4162G>T
|
XP_016872878.1:p.Ala1388Ser
|
|
XM_017017390.1:c.2479G>T
|
XP_016872879.1:p.Ala827Ser
|
|
NM_133266.5:c.2425G>T
|
NP_573573.2:p.Ala809Ser
|
|
NR_110766.2:n.834+4199G>T
|
|
|
NM_001379226.1:c.3052G>T
|
NP_001366155.1:p.Ala1018Ser
|
|
NM_012309.5:c.4189G>T
MANE Select
|
NP_036441.2:p.Ala1397Ser
|
|