ENST00000281928.9:c.3310C>G
MANE Select
|
ENSP00000281928.3:p.Pro1104Ala
|
|
ENST00000549786.2:c.2738C>G
|
|
|
ENST00000648379.1:n.1678C>G
|
|
|
ENST00000648737.1:n.3074C>G
|
|
|
ENST00000648825.1:n.50C>G
|
|
|
ENST00000648916.1:n.1321C>G
|
|
|
ENST00000649607.1:c.1494C>G
|
|
|
ENST00000650226.1:c.3310C>G
|
ENSP00000496981.1:p.Pro1104Ala
|
|
ENST00000281928.7:c.3310C>G
|
ENSP00000281928.3:p.Pro1104Ala
|
|
NM_015335.4:c.3310C>G
|
NP_056150.1:p.Pro1104Ala
|
|
XM_011538080.1:c.3310C>G
|
XP_011536382.1:p.Pro1104Ala
|
|
XM_011538081.1:c.3307C>G
|
XP_011536383.1:p.Pro1103Ala
|
|
XM_011538082.1:c.3280C>G
|
XP_011536384.1:p.Pro1094Ala
|
|
XM_011538080.2:c.3310C>G
|
XP_011536382.1:p.Pro1104Ala
|
|
XM_011538081.2:c.3307C>G
|
XP_011536383.1:p.Pro1103Ala
|
|
XM_011538082.2:c.3280C>G
|
XP_011536384.1:p.Pro1094Ala
|
|
XM_017019090.1:c.3307C>G
|
XP_016874579.1:p.Pro1103Ala
|
|
NM_015335.5:c.3310C>G
MANE Select
|
NP_056150.1:p.Pro1104Ala
|
|