ENST00000224721.12:c.6318C>G
MANE Select
|
ENSP00000224721.9:p.Tyr2106Ter
|
|
ENST00000224721.10:c.6333C>G
|
ENSP00000224721.8:p.Tyr2111Ter
|
|
ENST00000622827.4:c.6318C>G
|
ENSP00000483211.1:p.Tyr2106Ter
|
|
NM_022124.5:c.6318C>G
|
NP_071407.4:p.Tyr2106Ter
|
|
XM_006717940.2:c.6513C>G
|
XP_006718003.1:p.Tyr2171Ter
|
|
XM_006717942.2:c.6447C>G
|
XP_006718005.1:p.Tyr2149Ter
|
|
XM_011540039.1:c.6510C>G
|
XP_011538341.1:p.Tyr2170Ter
|
|
XM_011540040.1:c.6507C>G
|
XP_011538342.1:p.Tyr2169Ter
|
|
XM_011540041.1:c.6453C>G
|
XP_011538343.1:p.Tyr2151Ter
|
|
XM_011540042.1:c.6513C>G
|
XP_011538344.1:p.Tyr2171Ter
|
|
XM_011540043.1:c.6513C>G
|
XP_011538345.1:p.Tyr2171Ter
|
|
XM_011540044.1:c.6378C>G
|
XP_011538346.1:p.Tyr2126Ter
|
|
XM_011540045.1:c.6513C>G
|
XP_011538347.1:p.Tyr2171Ter
|
|
XM_011540046.1:c.5973C>G
|
XP_011538348.1:p.Tyr1991Ter
|
|
XM_011540047.1:c.5331C>G
|
XP_011538349.1:p.Tyr1777Ter
|
|
XM_011540048.1:c.6513C>G
|
XP_011538350.1:p.Tyr2171Ter
|
|
XM_011540049.1:c.6513C>G
|
XP_011538351.1:p.Tyr2171Ter
|
|
XM_011540050.1:c.6513C>G
|
XP_011538352.1:p.Tyr2171Ter
|
|
XM_011540051.1:c.6513C>G
|
XP_011538353.1:p.Tyr2171Ter
|
|
XM_011540052.1:c.2841C>G
|
XP_011538354.1:p.Tyr947Ter
|
|
XR_945796.1:n.6756C>G
|
|
|
NM_022124.6:c.6318C>G
MANE Select
|
NP_071407.4:p.Tyr2106Ter
|
|