ENST00000265104.5:c.10915G>T
MANE Select
|
ENSP00000265104.4:p.Asp3639Tyr
|
|
ENST00000681290.1:c.10870G>T
|
ENSP00000505288.1:p.Asp3624Tyr
|
|
ENST00000265104.4:c.10915G>T
|
ENSP00000265104.4:p.Asp3639Tyr
|
|
NM_001369.2:c.10915G>T
|
NP_001360.1:p.Asp3639Tyr
|
|
XM_005248262.2:c.10870G>T
|
XP_005248319.1:p.Asp3624Tyr
|
|
XM_005248262.3:c.11023G>T
|
XP_005248319.2:p.Asp3675Tyr
|
|
XM_017009177.1:c.11023G>T
|
XP_016864666.1:p.Asp3675Tyr
|
|
XM_017009178.1:c.9928G>T
|
XP_016864667.1:p.Asp3310Tyr
|
|
XM_017009179.2:c.9928G>T
|
XP_016864668.1:p.Asp3310Tyr
|
|
XM_017009180.1:c.11023G>T
|
XP_016864669.1:p.Asp3675Tyr
|
|
XM_017009181.1:c.11023G>T
|
XP_016864670.1:p.Asp3675Tyr
|
|
XM_017009182.1:c.11023G>T
|
XP_016864671.1:p.Asp3675Tyr
|
|
XM_017009185.1:c.6112G>T
|
XP_016864674.1:p.Asp2038Tyr
|
|
XM_017009186.1:c.5665G>T
|
XP_016864675.1:p.Asp1889Tyr
|
|
XM_017009188.1:c.5002G>T
|
XP_016864677.1:p.Asp1668Tyr
|
|
XM_024454388.1:c.9928G>T
|
XP_024310156.1:p.Asp3310Tyr
|
|
XM_024454389.1:c.9517G>T
|
XP_024310157.1:p.Asp3173Tyr
|
|
NM_001369.3:c.10915G>T
MANE Select
|
NP_001360.1:p.Asp3639Tyr
|
|