ENST00000346208.4:c.687C>G
|
ENSP00000341619.3:p.Tyr229Ter
|
|
ENST00000379328.9:c.687C>G
MANE Select
|
ENSP00000368632.3:p.Tyr229Ter
|
|
ENST00000346208.3:c.687C>G
|
ENSP00000341619.3:p.Tyr229Ter
|
|
ENST00000379328.7:c.687C>G
|
ENSP00000368632.3:p.Tyr229Ter
|
|
ENST00000461472.1:n.352C>G
|
|
|
NM_001002295.1:c.687C>G
|
NP_001002295.1:p.Tyr229Ter
|
|
NM_002051.2:c.687C>G
|
NP_002042.1:p.Tyr229Ter
|
|
XM_005252442.2:c.687C>G
|
XP_005252499.1:p.Tyr229Ter
|
|
XM_005252443.3:c.687C>G
|
XP_005252500.1:p.Tyr229Ter
|
|
XM_005252443.5:c.687C>G
|
XP_005252500.1:p.Tyr229Ter
|
|
NM_001002295.2:c.687C>G
MANE Select
|
NP_001002295.1:p.Tyr229Ter
|
|
NM_002051.3:c.687C>G
|
NP_002042.1:p.Tyr229Ter
|
|