ENST00000224721.12:c.2058A>T
MANE Select
|
ENSP00000224721.9:p.Ala686=
|
|
ENST00000398809.9:c.2058A>T
|
ENSP00000381789.5:p.Ala686=
|
|
ENST00000442677.4:c.2058A>T
|
ENSP00000388894.3:p.Ala686=
|
|
ENST00000466757.8:c.1489A>T
|
|
|
ENST00000224721.10:c.2073A>T
|
ENSP00000224721.8:p.Ala691=
|
|
ENST00000299366.11:c.2058A>T
|
ENSP00000299366.8:p.Ala686=
|
|
ENST00000398809.8:c.2058A>T
|
ENSP00000381789.5:p.Ala686=
|
|
ENST00000442677.3:c.833A>T
|
|
|
ENST00000466757.7:c.1489A>T
|
|
|
ENST00000616684.4:c.2058A>T
|
ENSP00000482036.2:p.Ala686=
|
|
ENST00000622827.4:c.2058A>T
|
ENSP00000483211.1:p.Ala686=
|
|
NM_001171930.1:c.2058A>T
|
NP_001165401.1:p.Ala686=
|
|
NM_001171931.1:c.2058A>T
|
NP_001165402.1:p.Ala686=
|
|
NM_022124.5:c.2058A>T
|
NP_071407.4:p.Ala686=
|
|
XM_006717940.2:c.2253A>T
|
XP_006718003.1:p.Ala751=
|
|
XM_006717942.2:c.2187A>T
|
XP_006718005.1:p.Ala729=
|
|
XM_011540039.1:c.2253A>T
|
XP_011538341.1:p.Ala751=
|
|
XM_011540040.1:c.2247A>T
|
XP_011538342.1:p.Ala749=
|
|
XM_011540041.1:c.2193A>T
|
XP_011538343.1:p.Ala731=
|
|
XM_011540042.1:c.2253A>T
|
XP_011538344.1:p.Ala751=
|
|
XM_011540043.1:c.2253A>T
|
XP_011538345.1:p.Ala751=
|
|
XM_011540044.1:c.2118A>T
|
XP_011538346.1:p.Ala706=
|
|
XM_011540045.1:c.2253A>T
|
XP_011538347.1:p.Ala751=
|
|
XM_011540046.1:c.1713A>T
|
XP_011538348.1:p.Ala571=
|
|
XM_011540047.1:c.1071A>T
|
XP_011538349.1:p.Ala357=
|
|
XM_011540048.1:c.2253A>T
|
XP_011538350.1:p.Ala751=
|
|
XM_011540049.1:c.2253A>T
|
XP_011538351.1:p.Ala751=
|
|
XM_011540050.1:c.2253A>T
|
XP_011538352.1:p.Ala751=
|
|
XM_011540051.1:c.2253A>T
|
XP_011538353.1:p.Ala751=
|
|
XM_011540053.1:c.2253A>T
|
XP_011538355.1:p.Ala751=
|
|
XM_011540054.1:c.2193A>T
|
XP_011538356.1:p.Ala731=
|
|
XR_945796.1:n.2496A>T
|
|
|
NM_001171930.2:c.2058A>T
|
NP_001165401.1:p.Ala686=
|
|
NM_001171931.2:c.2058A>T
|
NP_001165402.1:p.Ala686=
|
|
NM_022124.6:c.2058A>T
MANE Select
|
NP_071407.4:p.Ala686=
|
|