ENST00000683611.1:n.1151C>G
|
|
|
ENST00000265104.5:c.13818C>G
MANE Select
|
ENSP00000265104.4:p.Ala4606=
|
|
ENST00000681290.1:c.13773C>G
|
ENSP00000505288.1:p.Ala4591=
|
|
ENST00000265104.4:c.13818C>G
|
ENSP00000265104.4:p.Ala4606=
|
|
NM_001369.2:c.13818C>G
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NP_001360.1:p.Ala4606=
|
|
XM_005248262.2:c.13773C>G
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XP_005248319.1:p.Ala4591=
|
|
XM_005248262.3:c.13926C>G
|
XP_005248319.2:p.Ala4642=
|
|
XM_017009177.1:c.13506C>G
|
XP_016864666.1:p.Ala4502=
|
|
XM_017009178.1:c.12831C>G
|
XP_016864667.1:p.Ala4277=
|
|
XM_017009179.2:c.12831C>G
|
XP_016864668.1:p.Ala4277=
|
|
XM_017009185.1:c.9015C>G
|
XP_016864674.1:p.Ala3005=
|
|
XM_017009186.1:c.8568C>G
|
XP_016864675.1:p.Ala2856=
|
|
XM_017009188.1:c.7905C>G
|
XP_016864677.1:p.Ala2635=
|
|
XM_024454388.1:c.12831C>G
|
XP_024310156.1:p.Ala4277=
|
|
XM_024454389.1:c.12420C>G
|
XP_024310157.1:p.Ala4140=
|
|
NM_001369.3:c.13818C>G
MANE Select
|
NP_001360.1:p.Ala4606=
|
|