|
ENST00000224721.12:c.6479T>C
MANE Select
|
ENSP00000224721.9:p.Val2160Ala
|
|
|
ENST00000224721.10:c.6494T>C
|
ENSP00000224721.8:p.Val2165Ala
|
|
|
ENST00000622827.4:c.6479T>C
|
ENSP00000483211.1:p.Val2160Ala
|
|
|
NM_022124.5:c.6479T>C
|
NP_071407.4:p.Val2160Ala
|
|
|
XM_006717940.2:c.6674T>C
|
XP_006718003.1:p.Val2225Ala
|
|
|
XM_006717942.2:c.6608T>C
|
XP_006718005.1:p.Val2203Ala
|
|
|
XM_011540039.1:c.6671T>C
|
XP_011538341.1:p.Val2224Ala
|
|
|
XM_011540040.1:c.6668T>C
|
XP_011538342.1:p.Val2223Ala
|
|
|
XM_011540041.1:c.6614T>C
|
XP_011538343.1:p.Val2205Ala
|
|
|
XM_011540042.1:c.6584T>C
|
XP_011538344.1:p.Val2195Ala
|
|
|
XM_011540043.1:c.6674T>C
|
XP_011538345.1:p.Val2225Ala
|
|
|
XM_011540044.1:c.6539T>C
|
XP_011538346.1:p.Val2180Ala
|
|
|
XM_011540045.1:c.6674T>C
|
XP_011538347.1:p.Val2225Ala
|
|
|
XM_011540046.1:c.6134T>C
|
XP_011538348.1:p.Val2045Ala
|
|
|
XM_011540047.1:c.5492T>C
|
XP_011538349.1:p.Val1831Ala
|
|
|
XM_011540048.1:c.6674T>C
|
XP_011538350.1:p.Val2225Ala
|
|
|
XM_011540049.1:c.6674T>C
|
XP_011538351.1:p.Val2225Ala
|
|
|
XM_011540050.1:c.6674T>C
|
XP_011538352.1:p.Val2225Ala
|
|
|
XM_011540051.1:c.6674T>C
|
XP_011538353.1:p.Val2225Ala
|
|
|
XM_011540052.1:c.3002T>C
|
XP_011538354.1:p.Val1001Ala
|
|
|
XR_945796.1:n.6917T>C
|
|
|
|
NM_022124.6:c.6479T>C
MANE Select
|
NP_071407.4:p.Val2160Ala
|
|
