ENST00000224721.12:c.6420C>A
MANE Select
|
ENSP00000224721.9:p.Tyr2140Ter
|
|
ENST00000224721.10:c.6435C>A
|
ENSP00000224721.8:p.Tyr2145Ter
|
|
ENST00000622827.4:c.6420C>A
|
ENSP00000483211.1:p.Tyr2140Ter
|
|
NM_022124.5:c.6420C>A
|
NP_071407.4:p.Tyr2140Ter
|
|
XM_006717940.2:c.6615C>A
|
XP_006718003.1:p.Tyr2205Ter
|
|
XM_006717942.2:c.6549C>A
|
XP_006718005.1:p.Tyr2183Ter
|
|
XM_011540039.1:c.6612C>A
|
XP_011538341.1:p.Tyr2204Ter
|
|
XM_011540040.1:c.6609C>A
|
XP_011538342.1:p.Tyr2203Ter
|
|
XM_011540041.1:c.6555C>A
|
XP_011538343.1:p.Tyr2185Ter
|
|
XM_011540042.1:c.6577+38C>A
|
XP_011538344.1:n.6577+38C>A
|
|
XM_011540043.1:c.6615C>A
|
XP_011538345.1:p.Tyr2205Ter
|
|
XM_011540044.1:c.6480C>A
|
XP_011538346.1:p.Tyr2160Ter
|
|
XM_011540045.1:c.6615C>A
|
XP_011538347.1:p.Tyr2205Ter
|
|
XM_011540046.1:c.6075C>A
|
XP_011538348.1:p.Tyr2025Ter
|
|
XM_011540047.1:c.5433C>A
|
XP_011538349.1:p.Tyr1811Ter
|
|
XM_011540048.1:c.6615C>A
|
XP_011538350.1:p.Tyr2205Ter
|
|
XM_011540049.1:c.6615C>A
|
XP_011538351.1:p.Tyr2205Ter
|
|
XM_011540050.1:c.6615C>A
|
XP_011538352.1:p.Tyr2205Ter
|
|
XM_011540051.1:c.6615C>A
|
XP_011538353.1:p.Tyr2205Ter
|
|
XM_011540052.1:c.2943C>A
|
XP_011538354.1:p.Tyr981Ter
|
|
XR_945796.1:n.6858C>A
|
|
|
NM_022124.6:c.6420C>A
MANE Select
|
NP_071407.4:p.Tyr2140Ter
|
|