ENST00000593993.7:c.700+421A>G
MANE Select
|
ENSP00000472165.2:n.700+421A>G
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ENST00000322153.11:c.700+421A>G
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ENSP00000314425.5:n.700+421A>G
|
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ENST00000593993.6:c.700+421A>G
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ENSP00000472165.2:n.700+421A>G
|
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ENST00000600835.6:c.700+421A>G
|
ENSP00000470788.1:n.700+421A>G
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NM_001290023.1:c.700+421A>G
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NP_001276952.1:n.700+421A>G
|
|
NM_001290024.1:c.820+421A>G
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NP_001276953.1:n.820+421A>G
|
|
NM_005535.2:c.700+421A>G
|
NP_005526.1:n.700+421A>G
|
|
NM_153701.2:c.700+421A>G
|
NP_714912.1:n.700+421A>G
|
|
XM_006722741.2:c.820+421A>G
|
XP_006722804.2:n.820+421A>G
|
|
XM_011527966.1:c.832+421A>G
|
XP_011526268.1:n.832+421A>G
|
|
XM_011527967.1:c.820+421A>G
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XP_011526269.1:n.820+421A>G
|
|
XM_011527968.1:c.832+421A>G
|
XP_011526270.1:n.832+421A>G
|
|
XM_011527969.1:c.820+421A>G
|
XP_011526271.1:n.820+421A>G
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|
XM_011527970.1:c.832+421A>G
|
XP_011526272.1:n.832+421A>G
|
|
XM_011527971.1:c.832+421A>G
|
XP_011526273.1:n.832+421A>G
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|
XM_011527972.1:c.832+421A>G
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XP_011526274.1:n.832+421A>G
|
|
XM_011527973.1:c.712+421A>G
|
XP_011526275.1:n.712+421A>G
|
|
XM_011527974.1:c.700+421A>G
|
XP_011526276.1:n.700+421A>G
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|
XM_011527975.1:c.820+421A>G
|
XP_011526277.1:n.820+421A>G
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|
XM_011527976.1:c.832+421A>G
|
XP_011526278.1:n.832+421A>G
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|
XM_011527977.1:c.820+421A>G
|
XP_011526279.1:n.820+421A>G
|
|
XM_006722741.3:c.820+421A>G
|
XP_006722804.2:n.820+421A>G
|
|
XM_011527966.2:c.832+421A>G
|
XP_011526268.1:n.832+421A>G
|
|
XM_011527967.2:c.820+421A>G
|
XP_011526269.1:n.820+421A>G
|
|
XM_011527968.3:c.832+421A>G
|
XP_011526270.1:n.832+421A>G
|
|
XM_011527969.2:c.820+421A>G
|
XP_011526271.1:n.820+421A>G
|
|
XM_011527970.2:c.832+421A>G
|
XP_011526272.1:n.832+421A>G
|
|
XM_011527971.3:c.832+421A>G
|
XP_011526273.1:n.832+421A>G
|
|
XM_011527972.3:c.832+421A>G
|
XP_011526274.1:n.832+421A>G
|
|
XM_011527973.2:c.712+421A>G
|
XP_011526275.1:n.712+421A>G
|
|
XM_011527974.2:c.700+421A>G
|
XP_011526276.1:n.700+421A>G
|
|
XM_011527975.2:c.820+421A>G
|
XP_011526277.1:n.820+421A>G
|
|
XM_011527976.2:c.832+421A>G
|
XP_011526278.1:n.832+421A>G
|
|
XM_011527977.2:c.820+421A>G
|
XP_011526279.1:n.820+421A>G
|
|
XM_017026762.1:c.97+421A>G
|
XP_016882251.1:n.97+421A>G
|
|
NM_001290023.2:c.700+421A>G
|
NP_001276952.1:n.700+421A>G
|
|
NM_005535.3:c.700+421A>G
MANE Select
|
NP_005526.1:n.700+421A>G
|
|
NM_153701.3:c.700+421A>G
|
NP_714912.1:n.700+421A>G
|
|