ENST00000318471.5:c.903+186C>G
MANE Select
|
ENSP00000315680.3:n.903+186C>G
|
|
ENST00000541292.6:c.*168+186C>G
|
ENSP00000441004.1:n.*168+186C>G
|
|
ENST00000678002.1:c.591+186C>G
|
|
|
ENST00000678557.1:c.789+186C>G
|
ENSP00000502962.1:n.789+186C>G
|
|
ENST00000679286.1:c.783+186C>G
|
ENSP00000503168.1:n.783+186C>G
|
|
ENST00000318471.4:c.903+186C>G
|
ENSP00000315680.3:n.903+186C>G
|
|
NM_000288.3:c.903+186C>G
|
NP_000279.1:n.903+186C>G
|
|
XM_005267019.3:c.789+186C>G
|
XP_005267076.1:n.789+186C>G
|
|
XM_006715502.1:c.609+186C>G
|
XP_006715565.1:n.609+186C>G
|
|
XM_005267019.4:c.789+186C>G
|
XP_005267076.1:n.789+186C>G
|
|
XM_006715502.2:c.609+186C>G
|
XP_006715565.1:n.609+186C>G
|
|
XM_017010934.2:c.*26+186C>G
|
XP_016866423.1:n.*26+186C>G
|
|
NM_000288.4:c.903+186C>G
MANE Select
|
NP_000279.1:n.903+186C>G
|
|