ENST00000338508.9:c.3415G>T
|
ENSP00000345193.7:p.Ala1139Ser
|
|
ENST00000412252.6:c.960G>T
|
ENSP00000414876.2:n.960G>T
|
|
ENST00000601538.6:c.5182G>T
MANE Select
|
ENSP00000469689.2:p.Ala1728Ser
|
|
ENST00000654939.1:c.2691G>T
|
|
|
ENST00000656230.1:c.4045G>T
|
ENSP00000499561.1:p.Ala1349Ser
|
|
ENST00000659264.1:c.3472G>T
|
ENSP00000499270.1:p.Ala1158Ser
|
|
ENST00000338508.8:c.3418G>T
|
ENSP00000345193.6:p.Ala1140Ser
|
|
ENST00000357171.7:c.*186G>T
|
ENSP00000349694.4:n.*186G>T
|
|
ENST00000409161.5:c.3394G>T
|
ENSP00000386491.1:p.Ala1132Ser
|
|
ENST00000412252.5:c.958G>T
|
|
|
ENST00000423696.6:c.4045G>T
|
ENSP00000394536.2:p.Ala1349Ser
|
|
ENST00000424924.5:c.3019G>T
|
ENSP00000402944.1:p.Ala1007Ser
|
|
ENST00000449833.6:c.3418G>T
|
ENSP00000399423.3:p.Ala1140Ser
|
|
ENST00000601538.5:c.5182G>T
|
ENSP00000469689.2:p.Ala1728Ser
|
|
ENST00000606715.3:n.1934G>T
|
|
|
NM_012309.4:c.5182G>T
|
NP_036441.2:p.Ala1728Ser
|
|
NM_133266.4:c.3418G>T
|
NP_573573.2:p.Ala1140Ser
|
|
NR_110766.1:n.1036G>T
|
|
|
XM_005277930.2:c.5182G>T
|
XP_005277987.1:p.Ala1728Ser
|
|
XM_005277932.2:c.4045G>T
|
XP_005277989.1:p.Ala1349Ser
|
|
XM_006718478.2:c.5152G>T
|
XP_006718541.1:p.Ala1718Ser
|
|
XM_011544854.1:c.5194G>T
|
XP_011543156.1:p.Ala1732Ser
|
|
XM_011544855.1:c.5173G>T
|
XP_011543157.1:p.Ala1725Ser
|
|
XM_011544856.1:c.5167G>T
|
XP_011543158.1:p.Ala1723Ser
|
|
XM_011544857.1:c.5146G>T
|
XP_011543159.1:p.Ala1716Ser
|
|
XM_011544859.1:c.4057G>T
|
XP_011543161.1:p.Ala1353Ser
|
|
XM_005277932.3:c.4045G>T
|
XP_005277989.1:p.Ala1349Ser
|
|
XM_017017387.1:c.5182G>T
|
XP_016872876.1:p.Ala1728Ser
|
|
XM_017017388.1:c.5182G>T
|
XP_016872877.1:p.Ala1728Ser
|
|
XM_017017389.1:c.5155G>T
|
XP_016872878.1:p.Ala1719Ser
|
|
XM_017017390.1:c.3472G>T
|
XP_016872879.1:p.Ala1158Ser
|
|
NM_133266.5:c.3418G>T
|
NP_573573.2:p.Ala1140Ser
|
|
NR_110766.2:n.1037G>T
|
|
|
NM_001379226.1:c.4045G>T
|
NP_001366155.1:p.Ala1349Ser
|
|
NM_012309.5:c.5182G>T
MANE Select
|
NP_036441.2:p.Ala1728Ser
|
|