ENST00000269217.11:c.789T>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Asn263Lys
|
|
ENST00000313654.14:c.5616T>G
MANE Select
|
ENSP00000324532.8:p.Asn1872Lys
|
|
ENST00000649721.1:c.2508T>G
|
ENSP00000497885.1:p.Asn836Lys
|
|
ENST00000269217.10:c.789T>G
|
ENSP00000269217.5:p.Asn263Lys
|
|
ENST00000313654.13:c.5616T>G
|
ENSP00000324532.8:p.Asn1872Lys
|
|
ENST00000399516.7:c.5616T>G
|
ENSP00000382432.2:p.Asn1872Lys
|
|
ENST00000586709.1:n.4T>G
|
|
|
ENST00000586751.5:c.394T>G
|
|
|
ENST00000587184.5:c.789T>G
|
ENSP00000466557.1:p.Asn263Lys
|
|
ENST00000588770.5:n.194T>G
|
|
|
NM_000227.4:c.789T>G
|
NP_000218.3:p.Asn263Lys
|
|
NM_001127717.2:c.5616T>G
|
NP_001121189.2:p.Asn1872Lys
|
|
NM_001127718.2:c.789T>G
|
NP_001121190.2:p.Asn263Lys
|
|
NM_198129.2:c.5616T>G
|
NP_937762.2:p.Asn1872Lys
|
|
XM_011525978.1:c.5643T>G
|
XP_011524280.1:p.Asn1881Lys
|
|
XM_011525979.1:c.5634T>G
|
XP_011524281.1:p.Asn1878Lys
|
|
XM_011525980.1:c.5625T>G
|
XP_011524282.1:p.Asn1875Lys
|
|
XM_011525981.1:c.5511T>G
|
XP_011524283.1:p.Asn1837Lys
|
|
XM_011525982.1:c.5643T>G
|
XP_011524284.1:p.Asn1881Lys
|
|
XM_011525978.2:c.5643T>G
|
XP_011524280.1:p.Asn1881Lys
|
|
XM_011525979.2:c.5634T>G
|
XP_011524281.1:p.Asn1878Lys
|
|
XM_011525980.2:c.5625T>G
|
XP_011524282.1:p.Asn1875Lys
|
|
XM_011525981.2:c.5511T>G
|
XP_011524283.1:p.Asn1837Lys
|
|
XM_011525982.2:c.5643T>G
|
XP_011524284.1:p.Asn1881Lys
|
|
XM_017025743.1:c.3495T>G
|
XP_016881232.1:p.Asn1165Lys
|
|
XM_017025744.1:c.1185T>G
|
XP_016881233.1:p.Asn395Lys
|
|
XR_001753199.1:n.5884T>G
|
|
|
NM_000227.5:c.789T>G
|
NP_000218.3:p.Asn263Lys
|
|
NM_001127717.3:c.5616T>G
|
NP_001121189.2:p.Asn1872Lys
|
|
NM_001127718.3:c.789T>G
|
NP_001121190.2:p.Asn263Lys
|
|
NM_198129.3:c.5616T>G
|
NP_937762.2:p.Asn1872Lys
|
|
NM_000227.6:c.789T>G
MANE Plus Clinical
|
NP_000218.3:p.Asn263Lys
|
|
NM_001127717.4:c.5616T>G
|
NP_001121189.2:p.Asn1872Lys
|
|
NM_001127718.4:c.789T>G
|
NP_001121190.2:p.Asn263Lys
|
|
NM_198129.4:c.5616T>G
MANE Select
|
NP_937762.2:p.Asn1872Lys
|
|