ENST00000265104.5:c.12609C>T
MANE Select
|
ENSP00000265104.4:p.Ala4203=
|
|
ENST00000681290.1:c.12564C>T
|
ENSP00000505288.1:p.Ala4188=
|
|
ENST00000265104.4:c.12609C>T
|
ENSP00000265104.4:p.Ala4203=
|
|
NM_001369.2:c.12609C>T
|
NP_001360.1:p.Ala4203=
|
|
XM_005248262.2:c.12564C>T
|
XP_005248319.1:p.Ala4188=
|
|
XM_005248262.3:c.12717C>T
|
XP_005248319.2:p.Ala4239=
|
|
XM_017009177.1:c.12717C>T
|
XP_016864666.1:p.Ala4239=
|
|
XM_017009178.1:c.11622C>T
|
XP_016864667.1:p.Ala3874=
|
|
XM_017009179.2:c.11622C>T
|
XP_016864668.1:p.Ala3874=
|
|
XM_017009180.1:c.12717C>T
|
XP_016864669.1:p.Ala4239=
|
|
XM_017009185.1:c.7806C>T
|
XP_016864674.1:p.Ala2602=
|
|
XM_017009186.1:c.7359C>T
|
XP_016864675.1:p.Ala2453=
|
|
XM_017009188.1:c.6696C>T
|
XP_016864677.1:p.Ala2232=
|
|
XM_024454388.1:c.11622C>T
|
XP_024310156.1:p.Ala3874=
|
|
XM_024454389.1:c.11211C>T
|
XP_024310157.1:p.Ala3737=
|
|
NM_001369.3:c.12609C>T
MANE Select
|
NP_001360.1:p.Ala4203=
|
|