ENST00000440460.7:c.1851T>G
MANE Select
|
ENSP00000394352.3:p.Asn617Lys
|
|
ENST00000440460.6:c.1851T>G
|
ENSP00000394352.3:p.Asn617Lys
|
|
ENST00000526500.5:n.847T>G
|
|
|
ENST00000615255.1:c.1218T>G
|
ENSP00000480808.1:p.Asn406Lys
|
|
ENST00000618522.4:n.1204T>G
|
|
|
NM_001037954.3:c.1851T>G
|
NP_001033043.1:p.Asn617Lys
|
|
NM_033425.4:c.1218T>G
|
NP_219493.1:p.Asn406Lys
|
|
XM_005277726.3:c.1851T>G
|
XP_005277783.1:p.Asn617Lys
|
|
XM_005277727.3:c.1848T>G
|
XP_005277784.1:p.Asn616Lys
|
|
XM_005277728.3:c.1218T>G
|
XP_005277785.1:p.Asn406Lys
|
|
XM_011543045.1:c.969T>G
|
XP_011541347.1:p.Asn323Lys
|
|
XM_011543046.1:c.963T>G
|
XP_011541348.1:p.Asn321Lys
|
|
XM_017018466.2:c.1848T>G
|
XP_016873955.1:p.Asn616Lys
|
|
XM_017018467.1:c.1848T>G
|
XP_016873956.1:p.Asn616Lys
|
|
XM_017018468.1:c.969T>G
|
XP_016873957.1:p.Asn323Lys
|
|
XM_017018469.1:c.963T>G
|
XP_016873958.1:p.Asn321Lys
|
|
XM_024448742.1:c.1743T>G
|
XP_024304510.1:p.Asn581Lys
|
|
XM_024448743.1:c.1740T>G
|
XP_024304511.1:p.Asn580Lys
|
|
NM_001037954.4:c.1851T>G
MANE Select
|
NP_001033043.1:p.Asn617Lys
|
|
NM_033425.5:c.1218T>G
|
NP_219493.1:p.Asn406Lys
|
|