ENST00000696290.1:c.2553T>G
MANE Select
|
ENSP00000512529.1:p.His851Gln
|
|
ENST00000155858.10:c.2553T>G
|
ENSP00000155858.5:p.His851Gln
|
|
ENST00000528453.1:c.2553T>G
|
ENSP00000436809.1:p.His851Gln
|
|
ENST00000533060.5:c.2553T>G
|
ENSP00000434121.1:p.His851Gln
|
|
ENST00000533881.5:c.2535T>G
|
ENSP00000434383.1:p.His845Gln
|
|
NM_014555.3:c.2553T>G
|
NP_055370.1:p.His851Gln
|
|
XM_011520035.1:c.2814T>G
|
XP_011518337.1:p.His938Gln
|
|
XM_017017628.1:c.2607T>G
|
XP_016873117.1:p.His869Gln
|
|
NM_014555.4:c.2553T>G
MANE Select
|
NP_055370.1:p.His851Gln
|
|