ENST00000369162.7:c.6527A>G
MANE Select
|
ENSP00000358159.2:p.Tyr2176Cys
|
|
ENST00000369162.6:c.6527A>G
|
ENSP00000358159.2:p.Tyr2176Cys
|
|
ENST00000518006.1:n.443A>G
|
|
|
NM_006828.3:c.6527A>G
|
NP_006819.2:p.Tyr2176Cys
|
|
XM_011535394.1:c.6542A>G
|
XP_011533696.1:p.Tyr2181Cys
|
|
XM_011535395.1:c.6233A>G
|
XP_011533697.1:p.Tyr2078Cys
|
|
XM_011535396.1:c.6233A>G
|
XP_011533698.1:p.Tyr2078Cys
|
|
XM_011535394.3:c.6542A>G
|
XP_011533696.1:p.Tyr2181Cys
|
|
XM_011535395.3:c.6233A>G
|
XP_011533697.1:p.Tyr2078Cys
|
|
XM_011535396.3:c.6233A>G
|
XP_011533698.1:p.Tyr2078Cys
|
|
XM_017010205.2:c.6233A>G
|
XP_016865694.1:p.Tyr2078Cys
|
|
XM_017010206.2:c.5108A>G
|
XP_016865695.1:p.Tyr1703Cys
|
|
XM_024446316.1:c.5729A>G
|
XP_024302084.1:p.Tyr1910Cys
|
|
NM_006828.4:c.6527A>G
MANE Select
|
NP_006819.2:p.Tyr2176Cys
|
|