ENST00000441802.7:c.12303C>T
MANE Select
|
ENSP00000406229.2:p.Gly4101=
|
|
ENST00000441802.6:c.12303C>T
|
ENSP00000406229.2:p.Gly4101=
|
|
ENST00000507105.1:c.99C>T
|
|
|
ENST00000507662.1:n.202C>T
|
|
|
ENST00000512347.1:n.495C>T
|
|
|
ENST00000614102.4:c.12309C>T
|
ENSP00000479573.1:p.Gly4103=
|
|
NM_005245.3:c.12303C>T
|
NP_005236.2:p.Gly4101=
|
|
XM_005262834.2:c.12303C>T
|
XP_005262891.1:p.Gly4101=
|
|
XM_005262835.1:c.12303C>T
|
XP_005262892.1:p.Gly4101=
|
|
XM_006714139.2:c.12303C>T
|
XP_006714202.1:p.Gly4101=
|
|
XM_005262834.3:c.12303C>T
|
XP_005262891.1:p.Gly4101=
|
|
XM_005262835.2:c.12303C>T
|
XP_005262892.1:p.Gly4101=
|
|
XM_006714139.3:c.12303C>T
|
XP_006714202.1:p.Gly4101=
|
|
NM_005245.4:c.12303C>T
MANE Select
|
NP_005236.2:p.Gly4101=
|
|