ENST00000338508.9:c.3422C>G
|
ENSP00000345193.7:p.Thr1141Ser
|
|
ENST00000412252.6:c.967C>G
|
ENSP00000414876.2:n.967C>G
|
|
ENST00000601538.6:c.5189C>G
MANE Select
|
ENSP00000469689.2:p.Thr1730Ser
|
|
ENST00000654939.1:c.2698C>G
|
|
|
ENST00000656230.1:c.4052C>G
|
ENSP00000499561.1:p.Thr1351Ser
|
|
ENST00000659264.1:c.3479C>G
|
ENSP00000499270.1:p.Thr1160Ser
|
|
ENST00000338508.8:c.3425C>G
|
ENSP00000345193.6:p.Thr1142Ser
|
|
ENST00000357171.7:c.*193C>G
|
ENSP00000349694.4:n.*193C>G
|
|
ENST00000409161.5:c.3401C>G
|
ENSP00000386491.1:p.Thr1134Ser
|
|
ENST00000412252.5:c.965C>G
|
|
|
ENST00000423696.6:c.4052C>G
|
ENSP00000394536.2:p.Thr1351Ser
|
|
ENST00000424924.5:c.3026C>G
|
ENSP00000402944.1:p.Thr1009Ser
|
|
ENST00000449833.6:c.3425C>G
|
ENSP00000399423.3:p.Thr1142Ser
|
|
ENST00000601538.5:c.5189C>G
|
ENSP00000469689.2:p.Thr1730Ser
|
|
ENST00000606715.3:n.1941C>G
|
|
|
NM_012309.4:c.5189C>G
|
NP_036441.2:p.Thr1730Ser
|
|
NM_133266.4:c.3425C>G
|
NP_573573.2:p.Thr1142Ser
|
|
NR_110766.1:n.1043C>G
|
|
|
XM_005277930.2:c.5189C>G
|
XP_005277987.1:p.Thr1730Ser
|
|
XM_005277932.2:c.4052C>G
|
XP_005277989.1:p.Thr1351Ser
|
|
XM_006718478.2:c.5159C>G
|
XP_006718541.1:p.Thr1720Ser
|
|
XM_011544854.1:c.5201C>G
|
XP_011543156.1:p.Thr1734Ser
|
|
XM_011544855.1:c.5180C>G
|
XP_011543157.1:p.Thr1727Ser
|
|
XM_011544856.1:c.5174C>G
|
XP_011543158.1:p.Thr1725Ser
|
|
XM_011544857.1:c.5153C>G
|
XP_011543159.1:p.Thr1718Ser
|
|
XM_011544859.1:c.4064C>G
|
XP_011543161.1:p.Thr1355Ser
|
|
XM_005277932.3:c.4052C>G
|
XP_005277989.1:p.Thr1351Ser
|
|
XM_017017387.1:c.5189C>G
|
XP_016872876.1:p.Thr1730Ser
|
|
XM_017017388.1:c.5189C>G
|
XP_016872877.1:p.Thr1730Ser
|
|
XM_017017389.1:c.5162C>G
|
XP_016872878.1:p.Thr1721Ser
|
|
XM_017017390.1:c.3479C>G
|
XP_016872879.1:p.Thr1160Ser
|
|
NM_133266.5:c.3425C>G
|
NP_573573.2:p.Thr1142Ser
|
|
NR_110766.2:n.1044C>G
|
|
|
NM_001379226.1:c.4052C>G
|
NP_001366155.1:p.Thr1351Ser
|
|
NM_012309.5:c.5189C>G
MANE Select
|
NP_036441.2:p.Thr1730Ser
|
|