|
NM_004304.5:c.1441A>T
MANE Select
|
NP_004295.2:p.Asn481Tyr
|
|
ENST00000389048.8:c.1441A>T
MANE Select
|
ENSP00000373700.3:p.Asn481Tyr
|
|
NM_004304.4:c.1441A>T
|
NP_004295.2:p.Asn481Tyr
|
|
ENST00000389048.7:c.1441A>T
|
ENSP00000373700.3:p.Asn481Tyr
|
|
ENST00000618119.4:c.310A>T
|
ENSP00000482733.1:p.Asn104Tyr
|
|
XR_001738688.2:n.2371A>T
|
|
|
XR_244977.3:n.560+883T>A
|
|
|
XR_244977.4:n.459+883T>A
|
|
|
XR_939920.1:n.584-623T>A
|
|
|
XR_939920.2:n.474-623T>A
|
|
|
XR_939921.1:n.572-623T>A
|
|
|
XR_939921.2:n.468-623T>A
|
|
|
XR_939922.1:n.563-623T>A
|
|
|
XR_939922.2:n.462-623T>A
|
|
|
XR_939923.1:n.563-623T>A
|
|
|
XR_939923.3:n.462-623T>A
|
|
|
XR_939924.1:n.563-623T>A
|
|
|
XR_939924.2:n.462-623T>A
|
|
|
XR_939925.1:n.560+883T>A
|
|
|
XR_939925.2:n.459+883T>A
|
|
|
XR_939926.1:n.560+883T>A
|
|
|
XR_939926.2:n.459+883T>A
|
|