ENST00000683611.1:n.1086C>G
|
|
|
ENST00000265104.5:c.13753C>G
MANE Select
|
ENSP00000265104.4:p.Pro4585Ala
|
|
ENST00000681290.1:c.13708C>G
|
ENSP00000505288.1:p.Pro4570Ala
|
|
ENST00000265104.4:c.13753C>G
|
ENSP00000265104.4:p.Pro4585Ala
|
|
NM_001369.2:c.13753C>G
|
NP_001360.1:p.Pro4585Ala
|
|
XM_005248262.2:c.13708C>G
|
XP_005248319.1:p.Pro4570Ala
|
|
XM_005248262.3:c.13861C>G
|
XP_005248319.2:p.Pro4621Ala
|
|
XM_017009177.1:c.13441C>G
|
XP_016864666.1:p.Pro4481Ala
|
|
XM_017009178.1:c.12766C>G
|
XP_016864667.1:p.Pro4256Ala
|
|
XM_017009179.2:c.12766C>G
|
XP_016864668.1:p.Pro4256Ala
|
|
XM_017009185.1:c.8950C>G
|
XP_016864674.1:p.Pro2984Ala
|
|
XM_017009186.1:c.8503C>G
|
XP_016864675.1:p.Pro2835Ala
|
|
XM_017009188.1:c.7840C>G
|
XP_016864677.1:p.Pro2614Ala
|
|
XM_024454388.1:c.12766C>G
|
XP_024310156.1:p.Pro4256Ala
|
|
XM_024454389.1:c.12355C>G
|
XP_024310157.1:p.Pro4119Ala
|
|
NM_001369.3:c.13753C>G
MANE Select
|
NP_001360.1:p.Pro4585Ala
|
|