ENST00000262493.12:c.812A>G
MANE Select
|
ENSP00000262493.6:p.Lys271Arg
|
|
ENST00000562316.6:c.479A>G
|
ENSP00000457238.2:p.Lys160Arg
|
|
ENST00000564727.2:c.116A>G
|
ENSP00000454971.2:p.Lys39Arg
|
|
ENST00000568375.2:c.116-3394A>G
|
|
|
ENST00000638185.1:n.1027A>G
|
|
|
ENST00000638210.1:n.1112A>G
|
|
|
ENST00000638705.1:c.812A>G
|
ENSP00000491223.1:p.Lys271Arg
|
|
ENST00000638836.1:n.722A>G
|
|
|
ENST00000639055.1:n.1533A>G
|
|
|
ENST00000639251.1:n.713A>G
|
|
|
ENST00000639268.1:c.447A>G
|
|
|
ENST00000639341.1:c.337A>G
|
|
|
ENST00000639770.1:c.850A>G
|
ENSP00000491999.1:n.850A>G
|
|
ENST00000640390.1:n.742A>G
|
|
|
ENST00000640469.1:c.176A>G
|
ENSP00000491875.1:p.Lys59Arg
|
|
ENST00000640560.1:n.588A>G
|
|
|
ENST00000640893.1:c.*210A>G
|
ENSP00000492677.1:n.*210A>G
|
|
ENST00000262493.10:c.812A>G
|
ENSP00000262493.6:p.Lys271Arg
|
|
ENST00000564727.1:c.32A>G
|
ENSP00000454971.1:p.Lys11Arg
|
|
ENST00000568375.1:n.116-3394A>G
|
|
|
NM_020988.2:c.812A>G
|
NP_066268.1:p.Lys271Arg
|
|
XM_011523003.1:c.686A>G
|
XP_011521305.1:p.Lys229Arg
|
|
XM_011523003.3:c.686A>G
|
XP_011521305.1:p.Lys229Arg
|
|
NM_020988.3:c.812A>G
MANE Select
|
NP_066268.1:p.Lys271Arg
|
|