ENST00000265104.5:c.12605G>A
MANE Select
|
ENSP00000265104.4:p.Gly4202Asp
|
|
ENST00000681290.1:c.12560G>A
|
ENSP00000505288.1:p.Gly4187Asp
|
|
ENST00000265104.4:c.12605G>A
|
ENSP00000265104.4:p.Gly4202Asp
|
|
NM_001369.2:c.12605G>A
|
NP_001360.1:p.Gly4202Asp
|
|
XM_005248262.2:c.12560G>A
|
XP_005248319.1:p.Gly4187Asp
|
|
XM_005248262.3:c.12713G>A
|
XP_005248319.2:p.Gly4238Asp
|
|
XM_017009177.1:c.12713G>A
|
XP_016864666.1:p.Gly4238Asp
|
|
XM_017009178.1:c.11618G>A
|
XP_016864667.1:p.Gly3873Asp
|
|
XM_017009179.2:c.11618G>A
|
XP_016864668.1:p.Gly3873Asp
|
|
XM_017009180.1:c.12713G>A
|
XP_016864669.1:p.Gly4238Asp
|
|
XM_017009185.1:c.7802G>A
|
XP_016864674.1:p.Gly2601Asp
|
|
XM_017009186.1:c.7355G>A
|
XP_016864675.1:p.Gly2452Asp
|
|
XM_017009188.1:c.6692G>A
|
XP_016864677.1:p.Gly2231Asp
|
|
XM_024454388.1:c.11618G>A
|
XP_024310156.1:p.Gly3873Asp
|
|
XM_024454389.1:c.11207G>A
|
XP_024310157.1:p.Gly3736Asp
|
|
NM_001369.3:c.12605G>A
MANE Select
|
NP_001360.1:p.Gly4202Asp
|
|