|
ENST00000395796.8:c.*1130G>T
|
ENSP00000379142.4:n.*1130G>T
|
|
|
ENST00000616242.5:c.*252G>T
|
ENSP00000482149.2:n.*252G>T
|
|
|
ENST00000683378.1:n.358G>T
|
|
|
|
ENST00000336642.9:c.166G>T
|
ENSP00000338009.5:p.Ala56Ser
|
|
|
ENST00000345378.7:c.1135G>T
|
ENSP00000223366.2:p.Ala379Ser
|
|
|
ENST00000403799.8:c.1132G>T
MANE Select
|
ENSP00000384247.3:p.Ala378Ser
|
|
|
ENST00000671824.1:c.1195G>T
|
ENSP00000500264.1:p.Ala399Ser
|
|
|
ENST00000672743.1:n.144G>T
|
|
|
|
ENST00000673284.1:c.1132G>T
|
ENSP00000499852.1:p.Ala378Ser
|
|
|
ENST00000336642.8:c.184G>T
|
ENSP00000338009.4:p.Ala62Ser
|
|
|
ENST00000345378.6:c.1135G>T
|
ENSP00000223366.2:p.Ala379Ser
|
|
|
ENST00000395796.7:c.1129G>T
|
ENSP00000379142.3:p.Ala377Ser
|
|
|
ENST00000403799.7:c.1132G>T
|
ENSP00000384247.3:p.Ala378Ser
|
|
|
ENST00000437084.1:c.1081G>T
|
ENSP00000402840.1:p.Ala361Ser
|
|
|
ENST00000459642.1:n.512G>T
|
|
|
|
ENST00000616242.4:c.1129G>T
|
ENSP00000482149.1:p.Ala377Ser
|
|
|
NM_000162.3:c.1132G>T
|
NP_000153.1:p.Ala378Ser
|
|
|
NM_033507.1:c.1135G>T
|
NP_277042.1:p.Ala379Ser
|
|
|
NM_033508.1:c.1129G>T
|
NP_277043.1:p.Ala377Ser
|
|
|
NM_000162.4:c.1132G>T
|
NP_000153.1:p.Ala378Ser
|
|
|
NM_001354800.1:c.1132G>T
|
NP_001341729.1:p.Ala378Ser
|
|
|
NM_001354801.1:c.121G>T
|
NP_001341730.1:p.Ala41Ser
|
|
|
NM_001354802.1:c.-9G>T
|
NP_001341731.1:n.-9G>T
|
|
|
NM_001354803.1:c.166G>T
|
NP_001341732.1:p.Ala56Ser
|
|
|
NM_033507.2:c.1135G>T
|
NP_277042.1:p.Ala379Ser
|
|
|
NM_033508.2:c.1129G>T
|
NP_277043.1:p.Ala377Ser
|
|
|
XM_024446707.1:c.-9G>T
|
XP_024302475.1:n.-9G>T
|
|
|
NM_000162.5:c.1132G>T
MANE Select
|
NP_000153.1:p.Ala378Ser
|
|
|
NM_033507.3:c.1135G>T
|
NP_277042.1:p.Ala379Ser
|
|
|
NM_033508.3:c.1129G>T
|
NP_277043.1:p.Ala377Ser
|
|
|
NM_001354803.2:c.166G>T
|
NP_001341732.1:p.Ala56Ser
|
|
