ENST00000506729.6:c.1862T>A
MANE Select
|
ENSP00000421339.1:p.Val621Glu
|
|
ENST00000379807.7:c.1862T>A
|
ENSP00000369135.3:p.Val621Glu
|
|
ENST00000389019.7:c.1676T>A
|
ENSP00000373671.3:p.Val559Glu
|
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ENST00000506729.5:c.1862T>A
|
ENSP00000421339.1:p.Val621Glu
|
|
ENST00000513675.1:c.1103T>A
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ENSP00000421990.1:p.Val368Glu
|
|
ENST00000514765.6:n.232T>A
|
|
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NM_001289002.1:c.1862T>A
|
NP_001275931.1:p.Val621Glu
|
|
NM_001289004.1:c.1676T>A
|
NP_001275933.1:p.Val559Glu
|
|
NM_001308014.1:c.1103T>A
|
NP_001294943.1:p.Val368Glu
|
|
NM_173488.4:c.1862T>A
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NP_775759.3:p.Val621Glu
|
|
XM_005271874.2:c.1862T>A
|
XP_005271931.1:p.Val621Glu
|
|
XM_011543147.1:c.1757T>A
|
XP_011541449.1:p.Val586Glu
|
|
XM_011543148.1:c.1625T>A
|
XP_011541450.1:p.Val542Glu
|
|
XM_011543149.1:c.1289T>A
|
XP_011541451.1:p.Val430Glu
|
|
XM_011543150.1:c.1133T>A
|
XP_011541452.1:p.Val378Glu
|
|
XM_011543151.1:c.1103T>A
|
XP_011541453.1:p.Val368Glu
|
|
XM_011543153.1:c.1040T>A
|
XP_011541455.1:p.Val347Glu
|
|
XM_005271874.3:c.1862T>A
|
XP_005271931.1:p.Val621Glu
|
|
XM_011543147.2:c.1757T>A
|
XP_011541449.1:p.Val586Glu
|
|
XM_011543148.2:c.1625T>A
|
XP_011541450.1:p.Val542Glu
|
|
XM_011543153.2:c.1040T>A
|
XP_011541455.1:p.Val347Glu
|
|
NM_001289002.2:c.1862T>A
|
NP_001275931.1:p.Val621Glu
|
|
NM_001289004.2:c.1676T>A
|
NP_001275933.1:p.Val559Glu
|
|
NM_001308014.2:c.1103T>A
|
NP_001294943.1:p.Val368Glu
|
|
NM_173488.5:c.1862T>A
MANE Select
|
NP_775759.3:p.Val621Glu
|
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