ENST00000269217.11:c.2899A>C
MANE Plus Clinical
|
ENSP00000269217.5:p.Asn967His
|
|
ENST00000313654.14:c.7726A>C
MANE Select
|
ENSP00000324532.8:p.Asn2576His
|
|
ENST00000649721.1:c.4321A>C
|
ENSP00000497885.1:p.Asn1441His
|
|
ENST00000269217.10:c.2899A>C
|
ENSP00000269217.5:p.Asn967His
|
|
ENST00000313654.13:c.7726A>C
|
ENSP00000324532.8:p.Asn2576His
|
|
ENST00000399516.7:c.7558A>C
|
ENSP00000382432.2:p.Asn2520His
|
|
ENST00000586751.5:c.2504A>C
|
|
|
ENST00000587184.5:c.2731A>C
|
ENSP00000466557.1:p.Asn911His
|
|
ENST00000588770.5:n.2304A>C
|
|
|
NM_000227.4:c.2899A>C
|
NP_000218.3:p.Asn967His
|
|
NM_001127717.2:c.7558A>C
|
NP_001121189.2:p.Asn2520His
|
|
NM_001127718.2:c.2731A>C
|
NP_001121190.2:p.Asn911His
|
|
NM_198129.2:c.7726A>C
|
NP_937762.2:p.Asn2576His
|
|
XM_011525978.1:c.7753A>C
|
XP_011524280.1:p.Asn2585His
|
|
XM_011525979.1:c.7744A>C
|
XP_011524281.1:p.Asn2582His
|
|
XM_011525980.1:c.7735A>C
|
XP_011524282.1:p.Asn2579His
|
|
XM_011525981.1:c.7621A>C
|
XP_011524283.1:p.Asn2541His
|
|
XM_011525982.1:c.7456A>C
|
XP_011524284.1:p.Asn2486His
|
|
XM_011525978.2:c.7753A>C
|
XP_011524280.1:p.Asn2585His
|
|
XM_011525979.2:c.7744A>C
|
XP_011524281.1:p.Asn2582His
|
|
XM_011525980.2:c.7735A>C
|
XP_011524282.1:p.Asn2579His
|
|
XM_011525981.2:c.7621A>C
|
XP_011524283.1:p.Asn2541His
|
|
XM_011525982.2:c.7456A>C
|
XP_011524284.1:p.Asn2486His
|
|
XM_017025743.1:c.5605A>C
|
XP_016881232.1:p.Asn1869His
|
|
XM_017025744.1:c.3295A>C
|
XP_016881233.1:p.Asn1099His
|
|
XR_001753199.1:n.7994A>C
|
|
|
NM_000227.5:c.2899A>C
|
NP_000218.3:p.Asn967His
|
|
NM_001127717.3:c.7558A>C
|
NP_001121189.2:p.Asn2520His
|
|
NM_001127718.3:c.2731A>C
|
NP_001121190.2:p.Asn911His
|
|
NM_198129.3:c.7726A>C
|
NP_937762.2:p.Asn2576His
|
|
NM_000227.6:c.2899A>C
MANE Plus Clinical
|
NP_000218.3:p.Asn967His
|
|
NM_001127717.4:c.7558A>C
|
NP_001121189.2:p.Asn2520His
|
|
NM_001127718.4:c.2731A>C
|
NP_001121190.2:p.Asn911His
|
|
NM_198129.4:c.7726A>C
MANE Select
|
NP_937762.2:p.Asn2576His
|
|