ENST00000342741.6:c.951C>G
MANE Select
|
ENSP00000339933.4:p.His317Gln
|
|
ENST00000342741.4:c.951C>G
|
ENSP00000339933.4:p.His317Gln
|
|
ENST00000392414.7:c.858C>G
|
ENSP00000376214.3:p.His286Gln
|
|
NM_000298.5:c.951C>G
|
NP_000289.1:p.His317Gln
|
|
NM_181871.3:c.858C>G
|
NP_870986.1:p.His286Gln
|
|
XM_005245266.3:c.1110C>G
|
XP_005245323.1:p.His370Gln
|
|
XM_006711386.2:c.759C>G
|
XP_006711449.1:p.His253Gln
|
|
XM_011509639.1:c.1110C>G
|
XP_011507941.1:p.His370Gln
|
|
XM_011509640.1:c.759C>G
|
XP_011507942.1:p.His253Gln
|
|
NM_000298.6:c.951C>G
MANE Select
|
NP_000289.1:p.His317Gln
|
|
XM_006711386.4:c.759C>G
|
XP_006711449.1:p.His253Gln
|
|
XM_011509640.3:c.759C>G
|
XP_011507942.1:p.His253Gln
|
|
XM_017001493.1:c.951C>G
|
XP_016856982.1:p.His317Gln
|
|
NM_181871.4:c.858C>G
|
NP_870986.1:p.His286Gln
|
|