ENST00000696502.1:c.2483T>C
|
ENSP00000512668.1:p.Val828Ala
|
|
ENST00000696503.1:c.2546T>C
|
ENSP00000512669.1:p.Val849Ala
|
|
ENST00000696504.1:c.2546T>C
|
ENSP00000512670.1:p.Val849Ala
|
|
ENST00000676179.1:c.2621T>C
MANE Select
|
ENSP00000502065.1:p.Val874Ala
|
|
ENST00000263934.10:c.2483T>C
|
ENSP00000263934.6:p.Val828Ala
|
|
ENST00000377081.5:c.2621T>C
|
ENSP00000366284.1:p.Val874Ala
|
|
ENST00000377086.5:c.2621T>C
|
ENSP00000366290.1:p.Val874Ala
|
|
ENST00000620295.2:c.2579T>C
|
ENSP00000478500.1:p.Val860Ala
|
|
ENST00000622724.3:c.2543T>C
|
ENSP00000480063.1:p.Val848Ala
|
|
NM_015074.3:c.2483T>C , LRG_252t1:c.2483T>C
|
NP_055889.2:p.Val828Ala
|
|
NM_001365951.1:c.2621T>C
|
NP_001352880.1:p.Val874Ala
|
|
NM_001365952.1:c.2621T>C
|
NP_001352881.1:p.Val874Ala
|
|
NM_001365951.3:c.2621T>C
MANE Select
|
NP_001352880.1:p.Val874Ala
|
|